SCRS European Site Solutions Summit™

Adam Penna has been in clinical research for over 9 years. He has a background in finance and corporate law and has previously worked with a US healthcare access non-profit. Adam is presently an Associate Director, Clinical Operations at Merck overseeing a team of Clinical Operations Managers who work with clinical trials sites to negotiate…

Adam Cribbs brings over 20 years of experience in clinical research, including 15 years specializing in Start-Up and Site Activation. Adam has overseen Phase 1-4 studies, and all major therapeutic, driving operational excellence and efficiency, including significant experience in site and customer partnerships. Adam’s career journey—from Clinical Research Associate to Global Start-Up Leadership to North…

Adam is an executive leader and adjunct faculty member with over 15 years of experience in clinical research, spanning roles in academia, sponsor organizations, CROs, sites, tech companies, and retail pharmacy. He currently serves as Head of Clinical Delivery Operations at Walgreens, where he leads the development and execution of clinical trials across a national…

Adele Stevenson-Lampard is Director of Patient Concierge Services at Syneos Health, where she leads global patient support operations spanning travel, reimbursement, visit scheduling and call centre services across more than 40 countries. Her work focuses on simplifying the experience of clinical trial participation for patients while aiming to ease the operational burden placed on research…

With a career spanning over two decades in the healthcare industry, Alexandra has built a strong foundation of leadership, innovation, and dedication to advancing clinical research. Since beginning her research journey in 2009, she has held various roles that have shaped her into a strategic leader, now steering Ascend Clinical Research toward global recognition. Under…

Alexandra Gerritsen is the Founder and CEO of UniTriTeam, a consultancy that provides technology-driven support for clinical research sites across the country. With over 20 years of experience in technology and operations within highly regulated sectors like clinical research, Alexandra specializes in helping sites streamline operations, integrate advanced technologies, and scale efficiently. Before founding UniTriTeam,…

Alexandra Gerritsen is a global healthcare executive, entrepreneur, and sought-after speaker known for building scalable, high-performing organizations in the clinical research industry. She is the Founder and Co-CEO of UniTriTeam, a global staffing, technology implementation, and operational consulting firm dedicated to supporting clinical research sites and healthcare organizations across the United States and internationally. With…

Alexandria Clark is the co-owner and CEO of Administration at One of a Kind Clinical Research Center LLC. With a background in Biomedical Engineering, she oversees general administration of 1-OAK, her work focus’ on SOP development and implementation, patient connection and advocacy, and staff training and support. Alexandria holds a BSE degree and CCRC certification…

Alicia Staley serves as vice president of Patient Engagement at Medidata. She oversees the Patient Insights Program and the Patient Insights Board. She works to infuse the patient perspective throughout the product development lifecycle and help engage patients in novel ways.

Alisa is a dedicated professional with 28 years of experience in the clinical research field, where she has excelled in various roles with a strong emphasis on collaboration and strategic project management. Throughout her career, she has consistently delivered high-quality service and supported the successful conduct of studies. In her current role as Senior Site…

Alishia Ballintine is the Senior Manager, Legal and Compliance at University of the Sunshine Coast – Clinical Trials (UniSC CT). UniSC CT operates a clinical trial network across south-east Queensland, delivering clinical trials in collaboration with commercial sponsors across multiple therapeutic areas. In her role, Alishia provides strategic leadership across legal, regulatory, quality, and governance…

Alison Liddy, Senior Vice President at IQVIA for Patient and Site Centric Solutions, thrives on variety and challenge. With a career spanning over 20 years in the healthcare and life sciences industry, she excels in overseeing large global teams, P&L management, revenue growth, and C-Suite Relationship Management. Alison’s expertise extends to Digital & Change Transformation…

Alison has 25 years of experience developing complex integrated marcomms solutions across public and private sectors. Her portfolio highlights behavior change and social impact initiatives with government, nonprofit, philanthropy, academia, and above-brand Fortune 100-1000 companies. Alison’s focus areas are health equity (vaccines, chronic diseases, infectious diseases, impaired driving, cancer, reproductive health, domestic violence, gun violence…

Allyson Small is Chief Operating Officer of the Society for Clinical Research Sites (SCRS). With nearly 20 years of experience working in the healthcare industry, Small joined the SCRS team in 2013. She plays an integral role in strategic growth, developing key partnerships, and increasing global membership by 80%. Small also oversees all development and…

Allyson Small is the Chief Operating Officer of the Society for Clinical Research Sites (SCRS). With more than 20 years of experience working in the healthcare industry, Small joined the SCRS team in 2013. She plays an integral role in strategic growth, developing key partnerships, and increasing global membership. Small also oversees the development and…

Almenia Garvey brings over 25 years of expertise in Site and Investigator Relations, with a proven track record of driving global strategies that enhance clinical trial execution. In her current role as Sr. Director, Global Feasibility, Site and Patient Engagement at Allucent, Almenia leads the organization’s global site and patient engagement strategy, building robust site…

• Altair Silva is an Executive Director and Head of LOCATE at ThermoFisher Scientific, where he is also part of the Patient First Digital Solutions leadership team. A strategic leader with over 15 years of experience at the forefront of patient recruitment and retention, Altair has a proven track record of leading high-performing teams to…

Amanda has 18 years of experience in clinical research joining the Takeda Patient Recruitment & Retention team in August of 2019. Prior to her tenure with Takeda, she worked for several patient recruitment and retention agencies where she partnered with Sponsors, CROs and sites to design and implement multi-channel PR&R campaigns to meet the specialized…

Amanda Pickell is the Associate Director of Grant Payments at Fortrea, bringing over 15 years of experience in financial operations and clinical research support. She leads strategic initiatives to enhance the efficiency, transparency, and accuracy of site payments—ensuring that research partners are funded in a timely and consistent manner. Amanda is passionate about improving the…

Amanda Wright is a clinical research executive with over 25 years of experience forging shared-value strategic partnerships and collaborations to innovate business processes, patient engagement, and predictive modeling to drive more physician and patient participation in clinical research. A co-founder of Javara, she currently serves as Senior Vice President, Strategic Solutions. Amanda’s expertise includes clinical…

Medical Director and Principal Investigator leading Phase I–IV clinical studies at Paratus Clinical—known for quick start-up, steady recruitment, clear communication, and dependable delivery. Former GP and research chemist, combining real-world clinical care with research integrity to keep participants safe and studies on time with reliable data.

Dr. Fraser has decades of experience in clinical research. Currently, she is the Director- Clinical and Aerospace Health Research at the College of Medicine of the University of Central Florida.

Amy Jenkins joined Eli Lilly & Company in 2004 with over 12 years of clinical experience as an Acute Care Nurse Practitioner and now has more than 20 years in the pharmaceutical industry. Throughout her tenure, Amy has held various roles in medical and investigator engagement, including Clinical Development Liaison and Medical Science Liaison, significantly…

SCRS Committee Member and retired site founder. Dedicated to helping children, and parents through the Christina Gomez Foundation.

Transformation at the EMA where she leads the European clinical trials transformation initiative Accelerating Clinical Trials in the EU (ACT EU). In her role Ana also oversees the change management activities related to the implementation of the EU Clinical Trials Regulation and the Clinical Trials Information System (CTIS), and support to EU Member States. Prior…

En 2023 asumí el desafío de liderar Maffei e ICA como CEO, iniciando una etapa de expansión y profesionalización. Ser CEO en investigación clínica es habitar una intersección desafiante: El desarrollo de los protocolos, con tiempos de start up cada vez más ágiles, alto reclutamiento y datos de calidad. El liderazgo de equipos, el impacto…

Anahi Yañez is a recertified Specialist in Allergy and Clinical Immunology, is Medical Director and Principal Investigator of the Center for Research on Allergies and Respiratory Diseases – INAER, in Buenos Aires, Argentina, since 2006. She graduated from the Faculty of Medicine of the National University of Nordeste (UNNE) in 1982. She began her uninterrupted…

Anders Lindquist is a Senior Manager in Research Site Enablement in the field of Clinical Research (19 years). He has a Masters in Clinical Research Administration from Eastern Michigan University and obtained ACRP certification as a Certified Clinical Research Coordinator. At Labcorp, he has a special focus and passion for technology solutions and serves as…

Andrzej Schulz is a digital leader with more than 23 years of experience in IT, including over 13 years focused on data, analytics, and artificial intelligence initiatives across global organizations. His work centers on helping companies turn data into practical insights and scalable digital solutions. He currently serves as Head of Data, Analytics & AI…

Angela King, PhD, is a regulatory leader with over 15 years’ experience guiding regulatory strategy and delivery across multi country clinical trials in the EU and globally. She specialises in EU CTR execution, informed consent governance, and end to end clinical trial submission lifecycle management. Angela is known for driving lean process optimisation and supporting…

With extensive experience in global site relationship development and operations and specializing in organization, feasibility, proposal, and budget building, Angela is an expert at driving patient recruitment and identifying future research opportunities. She also brings deep oncology sales and marketing experience to identifying potential new market segments and leading oncology product sales teams. She finished…

Anna Fehr is the multi-site co-owner and CEO of operations at One of a Kind Clinical Research Center. With a research Career spanning over a decade, she oversees the daily operations of the research centers focusing on logistics, ALCOA practices, GCP adherence, patient care, regulatory compliance, trial startup, and provider engagement. Anna holds a bachelor’s…

Anna Fehr is the multi-site co-owner and CEO of operations at One of a Kind Clinical Research Center. With a research Career spanning over a decade, she oversees the daily operations of the research centers focusing on logistics, ALCOA practices, GCP adherence, patient care, regulatory compliance, trial startup, and provider engagement. Anna holds a bachelor’s…

Anna Megalakakis is a highly experienced clinical research professional and educator with over two decades of experience across the contract research organisation (CRO) and pharmaceutical sectors. As Associate Director of Education at ARCS Australia, she has held senior roles in clinical operations and training, developing deep expertise in drug development, regulatory compliance and Good Clinical…

I graduated from Kharkiv National Medical University and work as Professor Assoc. at Dnipro Institute of Medicine and Public Health. I have a PhD, Master of Medical and Educational Sciences, MBA, completed the internships at Harvard and Yale Universities, and I am a qualified international lecturer and senior researcher. I am an independent medical reviewer…

Anna Titkova, MD, PhD, Professor Assoc., MBA, International Operations Director Pratia, Country Head Ukraine Anna graduated from Kharkiv National Medical University and works here as a researcher and lecturer. She has a PhD, Master of Medical and Educational Sciences, MBA, completed an internship at Harvard and Yale Universities, and is a qualified international lecturer and…

Anne-Marie Baughn has been with Rx Trials for over 26 years. Anne-Marie has been Director of Business Development for Rx Trials for the past 24 years. She is primarily responsible for developing and indentifying clinical research opportunities and marketing Rx Trial’s clinical research sites to pharmaceutical and biotech companies, and clinical research organizations. Previously, Anne-Marie…

Dr. Anthony Avornyo is the Founder and Lead Principal Investigator of Ameli-BioGroup, a physician-led clinical research site established with the core intention of delivering high-quality, ethically grounded, and patient-centered clinical trials. With many years of experience in clinical research, Dr. Avornyo has led and overseen numerous studies across multiple therapeutic areas, building a strong reputation…

April Coburn has over 19 years’ experience in clinical research, working in a myriad of roles including Medical Writing, TMF Services, Clinical Operations, Global Study Start-Up, Global Site Relationships, Business Development, Site Services, and Physician Engagement.

I bring over 20 years of Clinical Research Experience within the Medical Device and Pharmaceutical industries, where my responsibilities have included designing, implementing and managing clinical studies that align with strategic goals and comply with regulations at both a local and international level. I have worked across all phases of clinical research and managed and…

Arjan is a seasoned Clinical Research Director with over 15 years of experience in the pharmaceutical industry. He has a background in paramedics and Health Sciences. Prior to joining MSD he held various roles at Sanofi and Wyeth. As a survivor of childhood cancer, Arjan understands the importance of clinical research and its impact. Leading…

Arjun Bhat is the Co-Founder and CEO of Clinrol, an AI-enabled clinical trial platform focused on improving how patients are identified, screened and engaged for research. He brings over 15 years of global clinical operations experience across oncology, vaccines, regenerative medicine and medical devices. He has held senior CRO and sponsor roles with organisations including…

Ash Clarke is a research management professional and currently the Director Research Operations at Grampians Health. With a strong commitment to advancing clinical trials and research in regional and rural Victoria, Ash is a passionate advocate for ensuring that rural and regional communities have access to innovative healthcare. Based in Ballarat, she brings extensive experience…

Ashley Moultrie is a clinical research leader with over 14 years of cross-functional experience spanning clinical operations, site leadership, and enterprise-level DEI & Community Engagement strategy. As Associate Director of Research Inclusion & Representation (RI&R) at Syneos Health, Ashley leads a global cross-functional team dedicated to advancing equitable access and inclusive practices across the clinical…

Ashley Moultrie is a seasoned professional with over 10 years of experience driving health equity through clinical research. As Associate Director of Clinical Trial Diversity (CTD) at Syneos Health, Ashley supports CTD leadership on strategic direction and partnership building to increase clinical trial participation for those with historically marginalized identities. A strong advocate for social…

As a senior product director with more than a decade of experience in the eCOA industry, Aubrey Verna has been instrumental in steering product development and innovation at YPrime. Aubrey’s experience is distinguished by a steadfast dedication to enhancing patient-centric trials through cutting-edge eCOA solutions, ensuring data integrity and adherence to regulatory standards. Aubrey’s pivotal…

Dr. Escobedo-Escotto holds a medical degree with a minor in Surgery from Guatemala, she received a master’s degree in public health fromt George Washington University. She has dedicated her last 8 years to the conduct and oversight of clinical research in the most underserved communities of the Washington D.C metro area. Her proficiency in English,…

Barney is the founder of Optimal Clinical Trials and currently works as a non executive Director of the NZCR group. The group includes NZCR, Optimal Clinical Trials, CMAX and Fusion covering specialist early phase units and separate late phase units across New Zealand and Australia. With over 20 years of medical experience, and investigator roles…

Barry Jacobson is a leading voice in transforming the Customer and Employee Experience. An accomplished executive, Barry offers a unique perspective—an insider’s view—From Main Street USA To Your Street™, focusing teams on building a culture of excellence. As the Chief Experience Officer of Barry Jacobson Consulting, Barry brings relevant experience and exceptional insight as it…

While running a research site, Barry Lake became frustrated with the manual methods and inefficiencies of managing the trial pipeline and study startup workflows and inability of any existing software to go beyond traditional CTMS to enable the capture and analysis of performance metrics to differentiate one site from the next. Finding no solution, Lake…

I am a medical graduate and a Certified Clinical Research Professional (CCRP) with 12 years of experience spanning both clinical practice and clinical research. Certified also as a Certified Professional in Healthcare Management (CPHM), I bring a strong operational background to my work. I began my career in family medicine, providing direct patient care for…

Blair Stevens is the Training Coordinator at Emeritus Research with over six years of experience in clinical research. Blair has worked across a range of roles at private sites, including Operations, Leadership, and Training, providing a broad perspective on the industry and its evolving needs. In her current role, she develops and manages site-wide training…

Bo Vaughan is a native of Richmond, VA and forward-thinking health care strategist with a track record for optimizing patient outcomes, improving the delivery of care, enhancing the patient experience while minimizing cost. Since the beginning of the COVID-19 pandemic, he has led schools, hospitals, and businesses to strategize on how best to mitigate the…

Brandon Freson is a Manager of Clinical Operations at Johnson & Johnson, based in Australia. He oversees clinical trial delivery across the immunology portfolio, with a strong focus on rapid study start‑up, site engagement, and recruitment performance. His work centers on partnering with clinical research sites to address operational barriers and improve trial execution. Having…

Brandon has over 25 years of experience in clinical research at site, CRO, and sponsor levels. Currently, he splits his time at Takeda as an Associate Director Study Site Engagement Lead and Diversity & Inclusion in Clinical Trials. Brandon is the acting Chair for the SCRS DSAT tool.

Bree Burks has held various roles including a bedside nurse, research coordinator, team manager and senior director of a large central clinical trials office across three leading academic medical centers. She has been responsible for over 1,000 trials spanning all translational stages across 38 unique clinical departments. She has developed and implemented many technical solutions…

Over the past 20+ years with CNS Healthcare, I’ve worked to develop an understanding of clinical trial site operations through progressive leadership roles, including CRC, Site Administrator, Director of Marketing, Clinical Development Liaison, and Director of Contracts & Trial Management. Each step has given me a deeper appreciation for what it takes to run a…

Brittaney Klocek is a Clinical Site Lead at Novo Nordisk with more than a decade of experience in clinical research, spanning site operations, start‑up, monitoring, and sponsor oversight. In her current role, Brittaney oversees site performance across the full clinical trial lifecycle, with a strong focus on start‑up excellence, risk mitigation, quality, and collaborative problem‑solving…

Brittany has been immersed in the clinical research industry for almost a decade, specifically within the site network space, where she’s held roles in both clinical operations and business development. She entered the field straight out of college and hasn’t looked back — clinical research has not only shaped her professional journey but continues to…

Candace Blackburn, RHIT, is a Research Charge Capture Specialist with Baptist Health, bringing more than 15 years of experience across patient access, prior authorization, revenue cycle operations, and clinical research billing. Her career has been shaped by working at the operational fault lines where study design, billing decisions, and real‑world site workflows intersect. Known for…

Carlos Orantes is the founding CEO of Alcanza Clinical Research. With 30+ years in life sciences, his expertise spans executive leadership, operational management, and process improvement. He has held key executive roles at Accelerated Enrollment Solutions, Meridien Research/Amplify Clinical, Accel Clinical, Frontage Laboratories, and other notable organizations. Carlos holds an MBA and a BS in…

Carlos Orantes is the founding CEO of Alcanza Clinical Research. With 30+ years in life sciences, his expertise spans executive leadership, operational management, and process improvement. He has held key executive roles at Accelerated Enrollment Solutions, Meridien Research/Amplify Clinical, Accel Clinical, Frontage Laboratories, and other notable organizations. Carlos holds an MBA and a BS in…

Carolyn Stewart has been the Business and Operations Manager of the Melbourne Children’s Trials Centre (MCTC) since its launch in 2014. MCTC is a collaboration between The Royal Children’s Hospital, Murdoch Children’s Research Institute, and the University of Melbourne which brings together a variety of support for all types of paediatric clinical research including trials….

With nearly 25 years of experience in the research site space, Casey has a long and exemplary career history in pharmaceutical research site services including serving as past President of the Society for Clinical Research Sites (SCRS), a global organization representing nearly 10,000 clinical research sites in 47 countries within the pharmaceutical industry. Casey began…

Cassie Kendrew is an experienced healthcare executive with a strong background in clinical research and healthcare delivery. As Chief Operating Officer at EMS Healthcare, Cassie leads the execution of clinical and commercial initiatives, ensuring the successful delivery of decentralised trials and mobile research solutions that improve patient access and engagement. With over a decade of…

Cate DiGirolamo, MBA, is the Financial Manager for the Genetics and Genomic Sciences Clinical Trials Office at the Icahn School of Medicine at Mount Sinai in New York City. In this role, she oversees financial operations and budgeting for a wide portfolio of clinical trials, supporting groundbreaking research at the intersection of genetics and medicine…

Catherine Gregor is a transformational leader and business advisor with close to two decades of experience in clinical research. She currently serves as the Chief Clinical Trial Officer for Florence Healthcare, a software company focused on connecting sponsors and sites worldwide. Catherine is a subject matter expert and key opinion leader on patient-centric, decentralized and…

Cheryl-Ann Hawkins is the Chief Executive Officer of Veritus Research and has had over 30 years in the health care industry, specifically, the last 20 years in clinical trials. Cheryl-Ann was appointed CEO of Veritus Research in October 2023 after being promoted from the COO role at sister company, Emeritus Research. Prior to her appointment…

Chloe Rose joined Pratia in 2021 and is the Executive Director of Portfolio Management – overseeing Global Feasibility & Proposals, Budget & Contract Negotiations, Early Phase Portfolio, and Global Client Relationship Management. Having prior experience from both Pharma and Academia, Chloe brings her passion to accelerate access to innovative treatments to patients through Pratia’s global…

Chloe Rose joined Pratia in 2021 and is the Executive Director of Portfolio Management – overseeing Global Feasibility & Proposals, Budget & Contract Negotiations, Early Phase Portfolio, and Global Client Relationship Management. Having prior experience from both Pharma and Academia, Chloe brings her passion to accelerate access to innovative treatments to patients through Pratia’s global…

Chris currently serves as Associate General Counsel, Privacy & AI at Medidata Solutions, Inc., a leading mission-driven life sciences platform transforming clinical development through data-driven AI. He manages the Privacy & AI legal team, which advises both internal and external stakeholders on a full range of complex data privacy, AI governance, and digital trust issues….

Chris Hoyle founded Elite Research Network in 2004 after working at a dedicated research site for 3 years where he was involved in all aspects of investigator site management, including patient recruitment, budgets and contracts, and business development. Since that time, Chris has been responsible for leading the direction and growth of the company. Chris…

With over three decades of diverse IT and strategic management experience, Chris Prader has been at the forefront of leading information technology for global companies as well as small firms alike. His career has taken him across Europe, Asia, and Australia, where he has lived and worked internationally, gaining invaluable insights and expertise. Chris has…

Serial entrepreneur and operator in the clinical trial space, Christian leads Populace Health, LLC, a global network of research sites that streamlines trial operations, centralizes infrastructure, and expands patient access—all while preserving site autonomy. He is also co-founder of ClinX, LLC (portfolio: ClinEdge, BTC Network, Guidestar Research), where he helped pioneer decentralized and direct-to-patient trials…

Professional working in trial management and engagement for Novo Nordisk Oceania. He has worked across a number of therapeutic areas within the Novo Nordisk portfolio from Obesity.

Christine Khoza has more than 23 years’ professional experience in clinical research. In her current position as Exec. Dir., Global Head, Study Start-Up & Site Intelligence at Allucent, she is responsible for managing and leading the study start-up activities within the Study Start-up (SSU) department of Allucent Clinical Trial Operations. She ensures planning, preparation and…

Dr. Christine Lee is a former FDA executive and nationally recognized leader in clinical trial innovation and workforce transformation. Her work is driven by one conviction: the future of clinical research depends on who’s leading it. During her tenure at the FDA, Dr. Lee directed over 80 studies designed to expand access, advance innovation, and…

Christine Senn, PhD is the SVP of Site-Sponsor Innovation at Advarra, a global company offering services and technology solutions to enable collaboration across all industry domains. She has worked in clinical research since 2005, starting at the University of Vermont College of Medicine then spent 16 years building the site network that became Centricity Research,…

Claire Finney is a strategic public health leader with a deep commitment to advancing health equity and inclusive research practices. As the Community Outreach and Engagement Manager for Sanofi’s Diversity & Inclusion in Clinical Trials team, Claire leads regional efforts across the Southeast to foster community trust, drive equitable participation in clinical trials, and operationalize…

Claire Gibson is the Director Clinical Operations (ANZ) at IQVIA, overseeing clinical trial operations for the full service business across Australia and New Zealand. With over 15 years of experience in the clinical research industry, Claire leads a team of approximately 180 professionals spanning feasibility, site identification, regulatory, and start-up, clinical monitoring and quality management….

Dr Claire Sears is the Head of Business Optimisation at EMS Healthcare, driving strategic initiatives to enhance healthcare accessibility. With over 20 years in pharmaceutical research, clinical technology, and academia, she is a leader in clinical trial technology and site engagement. Claire’s expertise spans site intelligence, product development, partnerships, and commercial strategy. Her background includes…

Dr Claire Sears is the Head of Business Optimisation at EMS Healthcare, driving strategic initiatives to enhance research and healthcare accessibility. With over 20 years in pharmaceutical research, clinical technology, and academia, she is a leader in clinical trial technology and site engagement. Claire’s expertise spans site intelligence, product development, partnerships, and commercial strategy. Her…

Dr. Grace is the CEO of EMS Healthcare, a unique and flexible Community Health Network which supports the delivery of clinical research and population health services and enables the provision of medical solutions deep within the heart of our communities. With a PhD in Molecular Oncology and over 20 years of experience in the biopharmaceutical…

Senior Manager, Strategic Planning at Tribe Clinical Research focused on scaling clinical research through innovation, technology, and operational efficiency. Leads cross-functional strategy across finance, operations, and leadership to evaluate growth opportunities, partnerships, and new capabilities. Work emphasizes advanced financial modeling, scenario analysis, and performance frameworks that translate complex data into clear, actionable decisions. Particularly focused…

I am the Director of Site Strategy & Engagement at Scout, where I lead global initiatives to enhance clinical trial delivery through effective site collaboration and strategic project execution. With nearly a decade of experience in clinical operations, project management, and laboratory management, I have had the opportunity to drive operational excellence and deliver successful…

I am the Director of Site Strategy & Engagement at Scout, where I lead global initiatives to enhance clinical trial delivery through effective site collaboration and strategic project execution. With nearly a decade of experience in clinical operations, project management, and laboratory management, I have had the opportunity to drive operational excellence and deliver successful…

Bi-lingual senior-level pharmaceutical professional with 37 years of experience serving four major life sciences organizations in local, regional, and global capacities. Possesses an excellent understanding of the rapidly evolving clinical research ecosystem and GxP quality & compliance environment. Broad experience in clinical trial management, clinical quality management, business process leadership, and regulatory authority inspections. Passionate…

Dan Milam is Co-Director of the Global Ambassador Program at the Society for Clinical Research Sites (SCRS), where he works to build a connected global network of site professionals and elevate the voice of clinical research sites worldwide. Through regional symposiums and strategic collaborations, he supports the sharing of insights, best practices, and emerging trends…

Dan Milam is the Founder and CEO of SiteEngage Solutions and serves as Co-Chair of the SCRS Ambassador Program, where he champions site advocacy and amplifies the voice of research sites globally. With over 30 years of experience working within the pharmaceutical, CRO, and clinical site sectors, Dan brings a uniquely well-rounded perspective on how…

Dan Otap is a Senior Alliance & Partnerships Lead within Genentech’s Research and Early Development unit (gRED). Dan’s clinical trial operations and compliance background uniquely position him to provide attuned insight into relational site engagement. Dan serves on various internal Roche/Genentech work streams related to clinical trial execution and innovation. He holds positions with the…

Dana Kudrnova has 17+ years working in the CRO industry – holding various positions including Senior Project Manager and Project Director. She successfully managed many phase I, II & III, global and international trials, as well as medical device studies for top pharmaceutical and biotech companies and ensured the highest level of the deliverables. In…

Daniel G Garza (he/him/él) brings over 20 years of advocacy, education, and unapologetic storytelling to Cheeky Charity’s Team. Diagnosed with AIDS in 2000 and anal cancer in 2015, Daniel has turned his personal health journey into a mission to empower others and spark conversations about HIV, cancer, and mental health. Through campaigns like Positively Fearless…

Results-driven and versatile Project Manager with experience in industry and government-sponsored clinical trials, Data Monitoring Committees (DMCs) and Project Management Offices (PMOs). My education background in business, life sciences and regulatory writing, coupled with a deep understanding of clinical trial protocols, has enabled me to effectively communicate and collaborate with cross-functional teams and stakeholders in…

Daniela Martinez, MSc, Associate Director of Clinical Operations, Argentina. Daniela Martinez holds a Master of Science degree in Biochemistry from the Universidad de Buenos Aires and has been recently certified as ontological coach, showcasing her commitment to continuous learning and professional development. With over 24 years of extensive experience in the clinical research field, Daniela…

Site Owner/Director since 1998 of a Phase I-IV, 25 employee, Multi-physician, Multi-specialty research site.

Darious Davis is a seasoned clinical research professional with a strong background in business development and trial operations. After a short stint in nursing, Darious transitioned into clinical research, where he has since built deep expertise in cultivating partnerships with contract research organizations, as well as pharmaceutical, biotech, and medical device companies. He currently serves…

Dave Hine spent the first half of his career working in the aerospace/defense industry as part of a software development team. While there, he learned about the process, training, and customer support required to make a software solution successful. Today, he applies that experience and passion to clinical trial financial software at Suvoda. He spends…

David Martinez is the CEO and co-founder of a growing independent clinical research site based in South Texas. With three years of experience in clinical trial leadership, David specializes in managing studies in obesity, diabetes, cardiovascular disease, and medical devices. Driven by a mission to expand access to research, his site operates in a medically…

David is a well-known thought leader and change agent in the clinical research industry through numerous associations, boards, initiatives, publications, presentations and contributions. A native of New Orleans, he has a Master’s degree in both Social Work and Business Administration and maintains the additional credentials of Certified IRB Professional (CIP), Regulatory Affairs Certification (RAC) and…

David is a well-known thought leader and change agent in the clinical research industry through numerous associations, boards, initiatives, publications, presentations and contributions. A native of New Orleans, he has a Master’s degree in both Social Work and Business Administration and maintains the additional credentials of Certified IRB Professional (CIP), Regulatory Affairs Certification (RAC) and…

David Burrow, Director of the FDA’s Office of Scientific Investigations (CDER), as he shares the agency’s outlook on advancing clinical trials through the Center for Clinical Trial Innovation (C3TI).

David Gebbo is a clinical research professional with a foundation in frontline healthcare and a strong appreciation for the connection between patient care and medical innovation. He began his career as a primary contact healthcare practitioner, developing expertise in diagnosing and treating neuro-musculoskeletal conditions and shaping a deeply patient-centric approach. He later transitioned into clinical…

Dave Hine spent the first half of his career working in the aerospace/defense industry as part of a software development team. While there, he learned about the process, training, and customer support required to make a software solution successful. Today, he applies that experience and passion to clinical trial financial software at Suvoda. He spends…

David is a well-known thought leader and change agent in the clinical research industry through numerous associations, boards, initiatives, publications, presentations and contributions. A native of New Orleans, he has a Master’s degree in both Social Work and Business Administration and maintains the additional credentials of Certified IRB Professional (CIP), Regulatory Affairs Certification (RAC) and…

Clinical Research Professional with strong strategic thinking skills who specializes in therapeutic networks, strategic alliances, and relationships with sites while leading a small team of Strategic Site Solutions Managers for US and Canada. Ability to build and grow therapeutic networks, specializing in cell and gene therapy, pediatrics, rare diseases, and MASH. Experience working cross-functionally to…

Deborah Clayton-Stamm is a Senior Clinical Operations Manager with extensive experience in the biotechnology sector, leading Phase I–III clinical trials across a range of therapeutic areas. Deborah oversees the Novotech Victorian CRA team and brings a people‑focused leadership approach to supporting and developing high‑performing teams. She works collaboratively with local early‑phase units to support high‑quality…

Debra Rogge, BSN, MSA, Director, AstraZeneca Pharmaceuticals. Debra holds a Bachelor of Science of Nursing and a Master of Science in Administration and Health care services. Debra‘s Clinical Research Experience has spanned numerous roles in the past 25 years both in the start-up and maintenance phases of sponsored and investigator sponsored studies. Debra’s current role…

Dr. Weinstein’s involvement in clinical research began in 2002 when she became involved as both a sub-investigator and principal investigator with Visions Clinical Research. In 2007, she founded her own clinical research company, ZASA Clinical Research which has had great success in all aspects of Internal Medicine research. In 2009, Dr. Weinstein co-founded and became…

Deena Bernstein has deep expertise in healthcare leadership and the clinical research industry. Her career spans over twenty years in clinical research site development, operations, and digital technology. Deena is a passionate leader with an entrepreneurial spirit who cares deeply about improving study participants’ clinical trial experience and process. Deena is Transformative Pharmaceutical Solutions (TPS) VP of…

Deena Bernstein has deep expertise in healthcare leadership and the clinical research industry. Her career spans over twenty years in clinical research site development, operations, and digital technology. Deena is a passionate leader with an entrepreneurial spirit who cares deeply about improving study participants’ clinical trial experience and process. Deena is Transformative Pharmaceutical Solutions (TPS) VP of…

Diana L. Foster, Ph.D., is a seasoned leader in the clinical research industry with a career spanning site ownership, global recruitment innovation, and executive leadership. Dr. Foster started her career in clinical trials on the clinical research side of the industry where she co-owned Metroplex Clinical Research Center in Dallas, TX. At that time, MCRC…

Diane Hardesty is a national speaker and patient advocate, using her family’s equally heartwarming and heartbreaking Lynch Syndrome hereditary cancer story of adversity and triumph to bring awareness of the importance of family cancer histories and germline genetic testing for hereditary cancer mutations. Before hereditary cancer genetic testing, there were 10 cancer deaths in Diane’s…

Dominique Barragan is an experienced clinical research leader with over 13 years of expertise in trial operations, team management, and regulatory compliance. She has successfully led multi-phase (I–IV) studies across a wide range of therapeutic areas, with a focus on operational excellence and patient-centered research. Known for building high-performing teams and navigating complex regulatory environments….

I am currently the Associated Director of Site Budgeting and Contracting at Takeda. I have over 15 years of experience in clinical research across Sites, CRO, and Sponsors. I started my career developing and negotiating site level oncology budgets, before gaining a broad range of experience in global study budget development and global site contract…

In his current role, Edward is leading Oncology Strategic Site Partnership within Global Site & Study Operations in R&D Pfizer. Driven by a deep passion for partnerships with sites and networks, Edward is committed to enhancing these key customizable strategic relationships, cultivating the best of science, medicine and operations for the treatment of all patients…

Eleanor Gibbons, BA, is currently a Clinical Research Manager for Sanford Health in Sioux Falls, SD. She began her research career in 2006 and has held MANY positions in Clinical Research since that time. She is passionate about Clinical Research and the difference it makes in the lives of patients, their families and future generations.

Dr. Elias Ketiar serves as the Clinical Vice President, Science & Medicine, at Signant Health. Dr. Ketiar draws on his wealth of more than 20 years of academic and clinical experience to advise on clinical trial design, execution, and governance. He has extensive experience in General Internal Medicine and Cardiology and is a Member of…

Elizabeth has been involved in clinical trials and drug development for over 27 years. Elizabeth has worked on all sides of the clinical trial portfolio – hospital (site) as clinical trials and therapeutic pharmacist for haematology/oncology/palliative care units; Project manager for Australian ASX listed biotech company Phase I First in Human to Phase II; Director…

Ellen Price is a clinical research leader with a 17-year career rooted in patient advocacy, community engagement, and participant-centered strategy. As Director of Patient Engagement at Tekton Research, she leads initiatives that amplify patient voices and drive meaningful change across clinical trial operations. Ellen facilitates Tekton’s monthly Patient and Partner Insight Committee, ensuring that real-world…

Dr Ellie Shingler is the Strategic Feasibility Manager at Boehringer Ingelheim UK & Ireland. Ellie leads the country and site-level clinical trial strategic feasibility assessment process within the UK and Ireland. In her role, she drives early engagement with external experts, centres of excellence, and patient organisations to enhance trial feasibility, start-up, and recruitment activities….

With over two decades of commercial experience, Eloise is highly skilled in implementing and executing business growth strategies, driving revenue, and providing solutions to facilitate successful clinical trials with a patient-centric approach. Her extensive tenure in the clinical research industry has fostered a profound passion for patient and site education and information, providing significant personal…

With nearly 20 years’ experience across academia, translational science, and clinical research education, Dr Eman Nafea is a recognised leader in research quality, workforce capability, accreditation, and national clinical research standards. Eman leads and advises on large‑scale education, GCP training, and accreditation initiatives that build sustainable workforce capability, align with NCTGF and international ICH‑GCP standards,…

Emery A. Noles, MSH, CCRP Vice President of Networking, ENCORE Research Group – A Division of Flourish Research Adjunct Instructor, Florida State College at Jacksonville Emery Noles is a seasoned clinical research professional with over 25 years of experience across academic, hospital, and private-sector research settings. As Vice President of Networking at ENCORE Research Group,…

Eric J. Rodriguez is an innovation strategist and keynote speaker who helps organizations lead people through rapid technological change in complex, high stakes environments. His career spans engineering, human resources, and global strategy, including fourteen years at Intel where he led large scale initiatives that supported communities across Arizona, Swaziland, and Ecuador. Throughout his work,…

Dr. Erik Buntinx, psychiatrist and founder of Anima, a private medical center with more than 500 patients under current treatment as well as an integrated clinical and pharmacological research unit, has studied several thousand patients in clinical trials for more than 30 years. These have often led to medications used worldwide. As a result, Dr….

Esther is a study start-up specialist at Aotearoa Clinical Trials.

Évelyne Newton is the Vice President of Business Development at Velocity Clinical Research. With over 20 years of experience in the healthcare and clinical research sector, she is responsible for leading key strategic partnerships and driving sales in Europe. Évelyne is also passionate about diversity, equity, inclusion, and belonging (DEIB), serving as the co-chair of…

Dr. Sandoval received his Bachelors of Science in molecular and cellular biology from Marymount University, and his Doctorate of Medicine from the Autonomous University of Guadalajara, School of Medicine. Before opening the doors to Emerson Clinical Research Institute (ECRI) Dr. Sandoval’s research activities have included bench research at the National Institutes of Neurological Disorders and…

Federica Bitonti is the Senior Director of Clinical Site Operations at Pfizer, leading the regional teams that partner directly with investigative sites to ensure smooth activation, clear communication, and high quality study conduct. She oversees Site Care Partners and Site Monitors, ensuring they provide timely guidance, resolve operational hurdles, and maintain transparent, consistent touchpoints for…

Gayna Whitaker has 25 years of clinical research experience and an MBA in Pharmaceutical Marketing and Healthcare Management. “It has always been my mission to educate the community about the clinical research process, to reduce healthcare disparities in the African American community and to be a voice for the underrepresented in clinical research. The industry…

I’ve been in this industry for more than 25 years starting as a CRA in pharma and then moving to a CRO and most recently as Director of Training for a large site network. I have a background in clinical research operations and learning and development. I hold a Combined Honours Bachelor of Science degree…

I’ve been in this industry for more than 25 years starting as a CRA in pharma and then moving to a CRO and most recently as Director of Quality Management and Training for a large site network. I have a background in clinical research operations and learning and development. I hold a Combined Honours Bachelor…

Dr. Georgina Sposetti is the Founder & CEO of Un Ensayo para Mí (“A Clinical Trial for Me”), the first patient-centric clinical-trial search and matching platform in Latin America that connects patients with investigators and research sites. She also serves as Director and Co-Founder of the Instituto de investigaciones clinicas in Mar del Plata, Argentina….

Gloria brings over 14 years of biopharma and CRO leadership across a broad range of therapeutic areas. Passionate about enhancing patient centricity and data driven approaches—especially in Asia Pacific—she currently drives Global Site Partnerships (GSP) to expand clinical trial access across cross regional sites and diverse communities. Her multilingual technical expertise and deep regional insights…

Grace Wong is the Quality, Training and Ethics Manager at Paratus Clinical Research, Australia, with nearly two decades of experience in the clinical research sector. Her expertise spans the management of large industry-sponsored trials, cooperative group studies, and investigator-initiated research, with a wide portfolio of clinical areas including early phase oncology trials. Committed to operational…

Greg Adams has over 20 years of experience in the pharmaceutical industry. Starting in the industry as a Research Pharmacist, he has broad expertise in Clinical Development, including all phases of clinical trials and has also held various roles in Clinical Pharmacology, the Pharmaceutical Sciences, and Discovery Research. He currently leads a site-facing team responsible…

17 years of experience managing site operations across regulatory, source, finance, recruitment, and clinical workflows. Oversees regulatory, eSource, eCRF data entry, contracts and budgets, information technology, as well as quality assurance. Holds a Masters in Pharmaceutical Sciences, Outcomes, and Policy with a Graduate certificate in Pharmaceutical Regulation as well as the rank of Eagle Scout.

Guillermo Ortiz is the General Manager, President and Founder of Fundación Estudios Clínicos, a non-profit organization with sites all over Argentina. Graduated from Universidad Austral, he has a bachelor’s degree in business administration. Throughout his career, Guillermo has founded various companies from construction to health providers. His true passion began when he founded his first…

Gwen Welty brings over 20 years of pharmaceutical industry R&D experience, six years at a major CRO, and currently serves as Executive Director leading the hyperCORE International site network team, which spans nine site networks across the US, Canada, Puerto Rico, and Ecuador, covering all therapeutic areas.

Haleh is a distinguished clinical research leader with extensive expertise spanning scientific research, clinical trial operations, and strategic health system leadership. She holds a PhD from the School of Medicine in England, a Master of Research in Stem Cell Research, and a degree in Genetics, reflecting a strong academic foundation in translational and biomedical science….

Dr. Hoeck is the Executive Clinical Director and Co-Founder of Future Medical Research. He has extensive senior clinical experience both as a clinician and scientist and Dr. Hoeck has served as Principal Investigator on investigator initiated and industry initiated studies from Phase I-IV. He has worked as a senior executive in the biopharmaceutical industry for…

Dr. Hoeck is the Executive Clinical Director and Co Founder of Future Medical Research. He has extensive senior clinical experience both as a clinician and scientist and Dr. Hoeck has served as Principal Investigator on investigator initiated and industry initiated studies from Phase I-IV. He has worked as a senior executive in the biopharmaceutical industry…

Heather O’Neal is a strategic Learning and Development leader with more than 20 years of experience driving organizational change through effective learning, communication, and engagement strategies. She currently serves as Director of Learning & Development at AMR Clinical, where she partners with executive leadership and cross-functional teams to lead enterprise learning initiatives that support business…

Heidi has over 18 years of experience in clinical research, with more than 15 years focused in site payments, financial operations, budget builds and negotiations. As the Associate Director of Clinical Study Site Payments at Takeda, she leads strategic initiatives to optimize investigator payments and improve site satisfaction. Throughout her career – spanning both CRO…

Henry Kravchenko is the founder and CEO of Clinical.ly, a technology company on a mission to deliver clinical research software that puts you in control. Clinical.ly works closely with the research community to understand its challenges and integrate its feedback into Clinical.ly’s intuitive, web-based technology solutions. This customer-centric approach ensures that Clinical.ly’s solutions truly address…

With almost 20 years in the clinical trials industry, I have enjoyed challenging and rewarding roles from Study Coordinator/Research Nurse, Senior CRA to Site Care Partner.

Holly Malin is the Head of Clinical Study Site Payments at Takeda. Holly has held a variety of leadership roles in Global Development Operations at Takeda over the past 14 years. Prior to her time at Takeda, she worked in R&D management consulting. She started her career working at clinical trial sites. Holly is passionate…

I start, run, and invest in companies – particularly those which advance healthcare by leveraging technology of all kinds. Specialties: Clinical trials, late phase drug development, drug safety, start-up organizations, drug development innovation. Increasingly interested in proteomics and monoclonal antibody based biotech start-ups – particularly those with candidates that need to get to Phase IB/IIA…

Iain Wood brings nearly 20 years of clinical research experience to his role as Senior Product Manager at Suvoda. Over the course of his career on the sponsor/pharma side, he specialized in and managed site budgeting and payment processes across multiple countries, developing deep expertise in the operational and financial complexities of global trials. During…

Dr. Ignacio MacKinnon has spent the past 20 years at the forefront of clinical research site at Instituto de Investigaciones Clínicas Mar del Plata, creating and leading a high-performing research organization dedicated to improve clinical trials performance. He is a physician, clinical researcher, Co-Founder and CEO of the site, which since 2006 conducted more than…

Isaac earned a PhD in Health Science from the University of Surrey in the UK and a master’s degree in public health and management from the Brighton and Sussex Institute of Post-Graduate Medicine. He was honoured with the Rosemary Pope Fund Award for his outstanding contributions to healthcare education and practice. Over 19 years, Isaac…

As an inclusion advocate, I am committed to being on the frontline in the fight for health equity. I currently work as an Associate Director of Clinical Operations, Diversity Program Lead at Merck. Formerly, I served on the Patient Inclusion and Health Equity team at Genentech’s Chief Diversity Office and then as a Clinical Trial…

Bella Tukuafu Johnson founded and leads Kalo Clinical Research with a clear purpose: protect people and progress science with integrity. Shaped by her upbringing in Punalu’u, Hawaii, her approach centers human dignity, inclusion, and authentic community connection so trials better reflect the people they are meant to serve.

Jade Tuttle is a versatile social work professional with 10+ years of experience in health equity, clinical trial diversity, and advocacy. As Director of Advocacy & Patient Affairs at Syneos Health, she leverages her expertise to integrate patient voices and advance inclusive drug development.

Jim DiCesare is passionate about delivering innovative clinical trial financial management solutions to investigator sites and sponsors. With over 25 years of industry experience leading clinical operations teams at Merck, CFS Clinical, DrugDev, and now IQVIA Jim has expertise across the contracting, budgeting, and investigator grant payment management continuum. He is a frequent speaker at…

James Riddle is the Senior Vice President of Global Review Operations at Advarra, the world’s largest provider of ethics, safety, and compliance oversight reviews services. With 25+ years’ experience providing support to the clinical research community, Riddle has operational responsibility for Advarra’s global review services including IRB, IBC, DMC, EAC. In this role, he helps…

Jan Hewett joined Advarra as the Senior Vice President, FDA Regulatory Advisor in May 2025. Prior to joining Advarra, Jan served as Regulatory Counsel (Policy) at the U.S. Food and Drug Administration’s Center for Drug Evaluation and Research (CDER) – Office of Compliance (OC) – Office of Scientific Investigations (OSI) for ten years. Jan has…

Jane has worked in clinical drug development for almost 30 years, starting her career at the bench at Eli Lilly. Over the course of her career she led clinical trials, registrational filing teams, molecular asset decision teams, and eventually led a global function focussed on driving cross-therapeutic area global patient recruitment. In her current role…

Janice Wiggins is the Vice President, Commercial at ObjectiveHealth, an integrated site network providing research opportunities as an extension of patient care and providing a custom-built technology platform to identify and stratify qualified research patients per protocol specifications. She has 23+ years of experience in both operational and commercial aspects of clinical research. She started…

Jean has been the Head of Site Operations at Rochester Clinical Research since 2024, and held roles in site operations since 2022. She has also served as an investigator on over 100 trials spanning a multi-therapeutic portfolio. She is a Physician Assistant with a master’s degree from Rochester Institute of Technology and is deeply passionate…

With more than 25 years of experience in the management of clinical trials, Jean-Marc joined Sanofi in 2008. First as Medical Advisor in Multiple Sclerosis in the Canadian Clinical Unit, then developing a strategic partnership with investigator sites across the globe, towards site optimization and performance, heading the Office of Global Site Partnership. Jean-Marc is…

With more than 25 years of experience in the management of clinical trials, phase I to IV, in various therapeutic areas and in the different environments of the industry: biotech, pharmaceutical and CRO, Jean-Marc joined Sanofi 15 years ago. First as Medical Advisor in MS in the Canadian CSU, then developing a strategic partnership with…

Jeff Huntsman is the Chief Commercial Officer, responsible for the overall commercial strategy and revenue generation for EmVenio Research. Mr. Huntsman joined EmVenio in 2024 with more than 30 years of experience in the Life Sciences space, where he has led global commercial teams selling pharma services and site solutions across the clinical development and…

A seasoned global executive with nearly two decades of leadership across clinical research and site operations.

Jeff Ventimiglia is the Senior Vice President of Offering & Portfolio Management at Medidata Solutions (A Dassault Systemes Company). An experienced business executive and life sciences consultant with 20 years of experience in product management, Life Sciences research, and technology deployment; Jeff has focused on driving better clinical trials and customer experience through the adoption…

Jeff Ventimiglia is the Senior Vice President of Offering & Portfolio Management at Medidata Solutions (A Dassault Systemes Company). An experienced business executive and life sciences consultant with 20 years of experience in product management, Life Sciences research, and technology deployment; Jeff has focused on driving better clinical trials and customer experience through the adoption…

Jeff Ventimiglia is the Senior Vice President of Offering & Portfolio Management at Medidata Solutions (A Dassault Systemes Company). An experienced business executive and life sciences consultant with 20 years of experience in product management, Life Sciences research, and technology deployment; Jeff has focused on driving better clinical trials and customer experience through the adoption…

With over 20 years of management and leadership experience in the healthcare industry, I oversee the daily operations and strategic development initiatives at TrueBlue Clinical Research, a multi-therapeutic clinical research site that provides high-quality and efficient services to sponsors and CROs. As certified clinical research professional I leverage my communication and discernment skills to build…

Jeffrey Zimmerman currently holds the position of Senior Director of Data Science and Application Development at Thermo Fisher Scientific’s PPD clinical research division. In this leading role, he has the crucial responsibility of incorporating a comprehensive range of AI/ML solutions and applications into clinical trial operations. Since joining the organization in 2016, Mr. Zimmerman has…

Dr Jelle Klein graduated as Medical Doctor in 2016 from the University of Antwerp with a Master of Science in Medicine. Between 2016 and 2018, he specialized in Obstetrics and Gynecology in several hospitals in Belgium. In 2024, he was recognized as a board-certified Clinical Pharmacologist. In October 2018, Dr Klein joined the SGS Phase…

Jenna Hove, RN has been a Clinical Research Director at Sanford Research since Summer 2021, overseeing Clinical Trial Operations & Pre-Award Financial teams. Prior to serving in this role, Jenna worked in a multitude of roles within the Clinical Research Department, including as a Clinical Research Coordinator, Project Manager, and Early Phase Research Manager gaining…

Jennifer Laws is an seasoned leader with over 17 years’ experience in clinical trial feasibility and site selection, specialising in optimising site selection strategies to ensure studies launch efficiently and meet enrolment goals. With a strong background in operational planning and data-driven decision making, she has spent her career bridging the gap between global trial…

Over 30 years of clinical research and nursing experience, with the majority of her career consisting of Site management and operations. Jennifer has initiated several clinical trial departments across the US, within academic medical centers, community health systems and private practice settings. She specializes in efficient clinical trial start-up, trial management, training and consulting. Expertise…

Jenny has a distinguished career in Clinical Research, with over 25 years of experience at the Respiratory Clinical Trials Unit (RCTU). As a Registered Nurse, her clinical expertise is complemented by her academic achievements, including a Master’s in Science (Research). Jenny’s wealth of knowledge makes her an invaluable resource for the entire RCTU team, and…

Jenny Peek is the Assistant Nursing Director for Clinical Trials at The Prince Charles Hospital (TPCH) and the operational lead of the TPCH Clinical Trials Centre (CTC). She led the establishment of the first dedicated CTC for TPCH and Metro North Health Service—Queensland’s largest health service—and is responsible for its ongoing operations and sustainability. Jenny…

Jesse Hoffman has been the Chief Business Officer at AMR Clinical, a prominent clinical research site company with 30+ locations across the United States, since 2019. With over 20 years of experience in the clinical research industry, Jesse has held significant site and CRO roles, including 12 years at Syneos Health, a global Contract Research…

Dr. Jhodie Duncan is the General Manager of Research and Partnerships at Latrobe Regional Health (LRH). She has over 25 year’s research experience having completed her PhD (Uni Melb) in the field of Developmental Neuroscience, after which she was awarded a CJ Martin Fellowship to undertake post-doctoral training at Boston’s Children’s Hospital/Harvard Medical School. In…

Jimmy Bechtel serves as the Chief Site Success Officer at the Society for Clinical Research Sites (SCRS), where he brings a rare blend of site-level experience and sponsor-side insight to the organization. His career began at the site level as a data specialist, patient recruiter, and operations manager, giving him firsthand knowledge of the daily…

Jimmy Bechtel serves as the Chief Site Success Officer at the Society for Clinical Research Sites (SCRS), where he brings a rare blend of site-level experience and sponsor-side insight to the organization. His career began at the site level as a data specialist, patient recruiter, and operations manager, giving him firsthand knowledge of the daily…

Jimmy Bechtel serves as the Chief Site Success Officer at the Society for Clinical Research Sites (SCRS), where he brings a rare blend of site-level experience and sponsor-side insight to the organization. His career began at the site level as a data specialist, patient recruiter, and operations manager, giving him firsthand knowledge of the daily…

Jimmy Bechtel serves as the Chief Site Success Officer at the Society for Clinical Research Sites (SCRS), where he brings a rare blend of site-level experience and sponsor-side insight to the organization. His career began at the site level as a data specialist, patient recruiter, and operations manager, giving him firsthand knowledge of the daily…

Joan Torony – March 2026 Joan is the Cluster Manager and Business Development Manager for Regional, Rural and Remote Clinical Trials Enabling Program Northern Cluster. She provides strategic advice on how to improve health inequity through consultation and engagement with key stakeholders to facilitate and establish clinical trial in RRR locations. With over 30 years’…

Joanne White is Associate Director, Resilience and Regional Clinical Operations at Moderna, where she supports strategic partnerships with investigative sites, contributes to feasibility and site selection, and helps drive successful clinical trial delivery across Australia and New Zealand. With more than 30 years of experience in the pharmaceutical and healthcare sectors, she brings deep expertise…

Joe Salmon is a Lead Research Nurse with extensive experience across a range of mental health and forensic care settings. Since qualifying as a Registered Mental Health Nurse, Joe has worked in Psychiatric Intensive Care Units (PICUs), forensic services, acute wards, liaison psychiatry, and research teams, building a strong foundation in complex clinical care and…

Joel develops global patient recruitment, retention, and engagement strategies for asset programs at Pfizer. Joel has spent the past 15 years dedicated to the field of patient recruitment. Starting his clinical research career at a site, it was from there he developed his commitment to make a difference to patients and sites globally. Joel is…

John is the Head of Decentralized Clinical Trials for Walgreens. In his role, he oversees research across a network of 20 pharmacy-based sites and a 50-state virtual site. He is passionate about empowering patient communities to become active participants at every stage of the clinical trial process. John has spent over a decade working at…

Jonathan is the CEO and Co-Founder at Stitch – The patient engagement platform for clinical trials. Stitch stops no shows, improves compliance and reduces manual work done by sites. He has 15 years experience in Life Sciences technology, in companies including, Veeva, uMotif, and IBM.

Jonathan is the CEO and Co-Founder at Stitch – The patient engagement platform for clinical trials. Stitch stops no shows, improves compliance and reduces manual work done by sites. He has 15 years experience in Life Sciences technology, in companies including uMotif, Veeva, and life sciences consulting at IBM.

Jonathan Patterson Business Development Associate and Director of Community Engagement at Quality Clinical Research. As a native resident in Omaha, Nebraska, my objective over the last three years has been to promote diversity and inclusion in clinical research by actively engaging and recruiting individuals from various backgrounds. My main goal has been to enhance healthcare…

With over two decades at the forefront of clinical operations excellence, Joe Cianciarulo embodies Sanofi’s commitment to chasing the miracles of science through patient-centered research innovation. As Head of the United States Clinical Study Unit, Joseph has transformed clinical research across multiple therapeutic areas, taking particular pride in his leadership roles contributing to the groundbreaking…

Joseph Kim has over 24 years of pharma research expertise. His career spans multiple Sponsors: Lilly, Merck and Takeda (Shire). Joe is recognized as a “Top 100 individual on the Medicine/Makers Power List,: and :20 Innovators Changing the Face of the Clinical Trials Industry” by CenterWatch.

Joseph Kim has over 25 years of pharma research expertise. His career spans multiple Sponsors: Lilly, Merck and Takeda (Shire). Joe is recognized as a “Top 100individual on the Medicine Makers Power List,” and “20Innovators Changing the Face of the Clinical Trials Industry” by CenterWatch.

Josie Harris is the Country Head for New Zealand at PPD, part of Thermo Fisher Scientific, where she leads one of the country’s largest CRO teams. She is a strong advocate for expanding local capabilities and strengthening New Zealand’s position as a competitive destination for global clinical trials. With leadership experience across large and mid-sized…

Josh is the Chief Technology Officer at ObjectiveHealth, a tech-enabled site network, where he leads technology strategy, engineering, and AI initiatives. With over 20 years in tech, including 15+ years in healthcare, Josh has applied his expertise in software engineering, solution architecture, systems integration, AI, and machine learning in the areas of population health, remote…

I am a Mexican physician dedicated to advancing clinical research with a focus on both scientific excellence and patient well-being. My career spans diverse therapeutic areas, where I have combined medical insight with leadership in site management, regulatory coordination, and cross-functional teamwork. I hold a Master’s degree in Health Institutions Management and a Graduate Specialization…

Justin Purvis is a seasoned clinical research leader with over a decade of experience in site contracts, investigator payments, and operational strategy. Currently serving as Senior Director of Site Contracts and Payments at PPD, Justin oversees global teams responsible for negotiating clinical trial agreements and managing payment operations across multiple studies. Since joining PPD in…

Justin Purvis is a seasoned clinical research leader with over a decade of experience in site contracts, investigator payments, and operational strategy. Currently serving as Senior Director of Site Contracts and Payments at PPD, Justin oversees global teams responsible for negotiating clinical trial agreements and managing payment operations across multiple studies. Since joining PPD in…

Kacey Murphy is Chief Commercial Officer at Momentum Clinical Research, where she leads all commercial functions, including business development, feasibility, marketing, and pricing. With over 20 years of experience across pharmaceuticals, medical devices, and clinical research, she brings deep understanding and delivery of clinical trials across diverse healthcare settings. Kacey has held senior roles at…

Kara Quinnelly is a clinical research professional with over 10 years of experience across a plethora of therapeutic areas. Kara provided both insight and support from site, CRO, and sponsor perspectives of the clinical research industry with previous roles in clinical operations, project delivery, and site engagement. Currently serving as an Associate Director for Site…

Karen McIntyre is Vice President, Global Site Alliances, Launch Excellence for Parexel. Her role is to provide strategic, site solution approaches to address the most critical challenges in the clinical trial pathway, predicable and successful patient recruitment. The driver of Global Site Alliances is to build and maintain purposeful relationships with sites to construct an…

Karen McIntyre is Vice President, Global Site Alliances, Launch Excellence for Parexel. Her role is to provide strategic, site solution approaches to address the most critical challenges in the clinical trial pathway, predicable and successful patient recruitment. The driver of Global Site Alliances is to build and maintain purposeful relationships with sites to construct an…

With a background in nursing, Karen joined the industry in 1992 as study site coordinator with extensive experience and expertise successfully managing the recruitment and maintenance of clinical trials across multiple therapeutic areas and phases. Karen has benefited from leadership roles within clinical operations, compliance management, and strategic relationships. She received her Master’s in Clinical…

Kari has over 15 years of experience across Phase I unit, operations, feasibility, and site strategy across APAC and England. Kari contributes extensively to Australia pre‑award and business development efforts, offering country‑specific feasibility insights and strategic input during bid defence meetings. Known for aligning study needs with site capabilities, Kari prioritises patient experience and long‑term…

Karim Chalhoub is the President and Chief Operating Officer of Alcanza Clinical Research. He has over 20 years of experience in healthcare, leading multi-site clinical operations and corporate development. Under his leadership, Alcanza has focused on building high-performance teams, optimizing study delivery, and enhancing the patient experience. Karim’s previous roles included COO at Caravel Autism…

Karri Venn brings over 25 years of clinical research experience working at clinical research sites. The ride has been monumental both in personal and professional growth. Ms. Venn started her career at LMC Healthcare in 1999 and that progressed to LMC Manna Research and ended with Centricity Research. A wide variety of positions Ms. Venn…

Karri Venn brings over 25 years of clinical research experience working at clinical research sites. The ride has been monumental both in personal and professional growth. Ms. Venn started her career at LMC Healthcare in 1999 and that progressed to LMC Manna Research and ended with Centricity Research. A wide variety of positions Ms. Venn…

Karri Venn brings over 25 years of clinical research experience working at clinical research sites. The ride has been monumental both in personal and professional growth. Ms. Venn started her career at LMC Healthcare in 1999 and that progressed to LMC Manna Research and ended with Centricity Research. A wide variety of positions Ms. Venn…

Karri Venn brings over 25 years of clinical research experience working at clinical research sites. The ride has been monumental both in personal and professional growth. Ms. Venn started her career at LMC Healthcare in 1999 and that progressed to LMC Manna Research and ended with Centricity Research. A wide variety of positions Ms. Venn…

Kasey brings over 15 years’ combined experience in the development and implementation of global clinical research programs. A large component of her work has been in translating scientific and market insights into enterprise-wide impact – supporting launch readiness, evidence generation, clinical development, and cross-functional portfolio execution. This includes leveraging technology to improve our understanding of…

My career in the clinical research industry began as a Regulatory Coordinator at an independent research site, where I gained firsthand experience with the operational and regulatory demands of clinical trials. Before joining Clinical.ly, I was a customer of the platform, which gave me a unique perspective on the challenges research sites face and the…

With a robust foundation in medical nutrition and wellness, Kathy has leveraged her healthcare knowledge and passion for data and technologies to forge a unique path in the clinical research space. She has 26 years of clinical site and CRO operations experience in the areas of business development, strategic feasibility, study start up, data management…

Kathy Mickel serves as the Director of Content and Engagement at the Society for Clinical Research Sites (SCRS), where she provides strategic leadership in developing Summit content and executing the SCRS Oncology Program and IncluDE Program. As a thought leader and strategic advisor, she shapes educational strategies, manages teams, and represents SCRS at industry events…

Kathy Mickel serves as the Director of Content and Engagement at the Society for Clinical Research Sites (SCRS), where she provides strategic leadership in developing Summit content and executing the SCRS Oncology Program and IncluDE Program. As a thought leader and strategic advisor, she shapes educational strategies, manages teams, and represents SCRS at industry events…

Kathy Mickel serves as the Director of Membership & Programs at the Society for Clinical Research Sites (SCRS), where she provides strategic leadership for member growth and engagement, and executing the SCRS Oncology Program and IncluDE Program. As a thought leader and strategic advisor, she shapes educational strategies, manages teams, and represents SCRS at industry…

Kathy Mickel serves as the Director of Content and Engagement at the Society for Clinical Research Sites (SCRS), where she provides strategic leadership in developing Summit content and executing the SCRS Oncology Program and IncluDE Program. As a thought leader and strategic advisor, she shapes educational strategies, manages teams, and represents SCRS at industry events…

Kaye Doiron is the founder and CEO of Research Works INC and Co-founder and CEO of SAMARAS, an AI-powered orchestration platform redefining how clinical trials are executed. A 17-year clinical trial site operator, she built and scaled a multi-site research network across New Orleans and San Juan without outside capital—serving diverse, often underrepresented populations across…

At Research Works, we’ve been passionate pioneers of medical advancement and uncompromising integrity for over 14 years. Our journey, initiated by our visionary CEO, Kaye Doiron, began in 2009 with a twofold mission: to address the under-representation of women in research and deliver unparalleled medical care to underserved communities. Today, our footprint spans from Louisiana…

Keith Karsten is the Chief Operating Officer of Clinical Research Billing, Inc., an outsourced financial management firm supporting independent research sites and large SMOs nationwide. With more than 16 years of experience in clinical research finance, he brings end-to-end expertise across the full clinical trial financial lifecycle, including 12 years negotiating and developing clinical trial…

Kelly Johnston McKee is a clinical research executive with more than 20 years of leadership in clinical innovation, optimization and site and patient engagement, known for building ecosystems that accelerate enrollment, reduce cost, and elevate the clinical trial experience. Kelly has led global initiatives spanning hybrid and decentralized trial execution, AI-supported enrollment workflows, site network…

Ken Getz is the Executive Director of the Tufts Center for the Study of Drug Development and a Research Professor at the Tufts University School of Medicine. He is an internationally recognized expert on pharmaceutical R&D management and execution, protocol design, contract service provider and investigative site management, eClinical technology and data usage, and patient…

Kerry Gorman, Senior Director, IQVIA has developed an understanding of clinical research and customer service through her past industry roles and current role as Head of IQVIA Strategic Site Solutions for US and Canada. Kerry leads a team of professionals at IQVIA who are passionate about sites, site concerns and continually focus on the development…

Kim Ribeiro, MLS (ASCP)CM, MS is an accomplished pharmaceutical executive with over 15 years of experience delivering high-impact, end-to-end solutions that drive significant value creation. Recognized for leading top-quartile performance, evidenced by accelerating or completing 85% of late-phase clinical trials in high-risk therapeutic areas, optimizing operational efficiency, and reducing timelines. Expert in driving organizational change…

Kim Ribeiro, MLS (ASCP)CM, MS is an accomplished pharmaceutical executive with over 15 years of experience delivering high-impact, end-to-end solutions that drive significant value creation. Recognized for leading top-quartile performance, evidenced by accelerating or completing 85% of late-phase clinical trials in high-risk therapeutic areas, optimizing operational efficiency, and reducing timelines. Expert in driving organizational change…

Kishor Rajendran serves as Head of Quality at Veritus Research, an early-phase clinical trials facility in Melbourne, where he leads quality management systems, regulatory compliance, and organizational excellence initiatives. With over 12 years of quality management experience spanning Food & Dairy, Engineering, Transfusion, Cell Therapy, and Early-phase Clinical Trials, he specializes in embedding innovative technologies…

With over 13 years of industry experience, Dr. Kristen Ballesteros is a results-oriented feasibility strategist and Director of Strategic Feasibility for Hematology/Oncology at PPD, part of Thermo Fisher Scientific. Her career provides a unique 360-degree view of clinical trial site selection, blending high-level corporate strategy with hands-on, site-level business development. From her vantage point at…

Kristi Robertson, Esq. is Senior Director, Clinical Trial Foundations, Community-Based Research Integration at Eli Lilly and Company. In this role, she leads efforts to embed community-based capabilities into clinical trial design and execution, helping ensure research is more inclusive and accessible to patients in real-world settings. She works across functions to integrate regulatory strategy, stakeholder…

Kristof Hadi is Associate Director, Study Site Engagement at Takeda, leading a regional team that supports clinical research sites across 12 Central and Eastern European countries. With more than 15 years of experience in clinical research, he focuses on strengthening sponsor–site collaboration, improving enrollment, and helping sites operate more efficiently in increasingly complex trials. He…

Laia Esteban Herrera, PhD, is Director of Site Support Solutions OUS at Care Access, where she leads the design and implementation of global site support services across international clinical trials. With more than 12 years of experience in clinical research across CRO and sponsor environments, Laia has played a key role in building scalable, site-centric…

Laia Esteban Herrera, PhD, is Director of Site Support Solutions OUS at Care Access, where she leads the design and implementation of global site support services across international clinical trials. With more than 12 years of experience in clinical research across CRO and sponsor environments, Laia has played a key role in building scalable, site-centric…

LaShell Robinson is the Head of :takeda: Diversity, Equity & Inclusion in the Clinical Research Department at Takeda. She leads a team dedicated to promoting education, awareness, and access through the “P.A.V.E.” program, aiming to eliminate barriers and expand opportunities in clinical research. LaShell’s journey began with volunteering at a research site, where she witnessed…

I direct the Center for Applied Clinical Research, which focuses on conducting phase 2, 3, and 4 clinical trials in obesity, diabetes, cardiology, nephrology, infectious diseases, pulmonology, and dermatology. With more than 20 years of experience and around 300 studies conducted, of which 61 are currently ongoing, we are a center of reference in our…

Laura Falcone, an advanced practice registered nurse (APRN), is a consultant with extensive clinical and operational expertise. Previously an executive at Velocity, she cultivated and managed strategic relationships with key sponsors and CROs. She has a sustained record of promoting patient‑centric research practices and has played a hands‑on role in overseeing day‑to‑day clinical operations, at…

I am an Oncology and Clinical Trials Pharmacy Manager with 6+ years’ experience, combined with proven ability to lead, support, manage, and mentor a team. I have strong experience in Oncology and Clinical Trials management, managing over 50 clinical trials on a day-to-day operational basis. Further, this extends from SSV, feasibility reviews, budget negotiation, SIV,…

Lauren Chazal, MBA is an expert in the clinical trials industry, with extensive experience in site operations, business development and financial management. She spent the initial five years of her career with traditional financial organizations and then pivoted to clinical research with a privately held multi-site clinical research organization. She has been instrumental in business…

Lauren Stockwell is a passionate and driven clinical research professional. As the Content & Engagement Manager for Society for Clinical Research Sites (SCRS), she works tirelessly to develop educational and mentorship programming to support the industry holistically. SCRS is the leading advocacy organization dedicated to unifying the voice of the global clinical research site community….

Lauren is a passionate and driven clinical research professional. As the Education & Engagement Manager for Society for Clinical Research Sites (SCRS), she works tirelessly to develop educational and mentorship programming to support the industry holistically. SCRS is the leading advocacy organization dedicated to unifying the voice of the global clinical research site community. Representing…

Lauren Stockwell is a passionate and driven clinical research professional. As the Content & Engagement Manager for Society for Clinical Research Sites (SCRS), she works tirelessly to develop educational and mentorship programming to support the industry holistically. SCRS is the leading advocacy organization dedicated to unifying the voice of the global clinical research site community….

Lauren Stockwell is a passionate and driven clinical research professional. As the Content & Engagement Manager for Society for Clinical Research Sites (SCRS), she works tirelessly to develop educational and mentorship programming to support the industry holistically. SCRS is the leading advocacy organization dedicated to unifying the voice of the global clinical research site community….

Lauri Befus serves as the Vice President of Clinical Operations at M3 Wake Research, one of the largest and most respected integrated site networks in the United States. With over 14 years of experience in clinical research and healthcare operations, Lauri leads multi-site strategies that bridge cutting-edge life sciences innovation with a deep commitment to…

Lee Eifler is an investor and serial entrepreneur. He has solved major challenges for pharma through first principles logic. He accelerated CV19 therapeutic study recruitment by harmonizing operations at testing facilities with the sites operating clinical studies. He then moved on to solving the participant diversity challenge by creating MACOA, Great Lakes Research Institute (acquired…

Lesley is currently the Associate Director of Product for IQVIA Technologies, Site and Planning Suite. She has over 15 years of industry experience with various perspectives, which she has gained from multiple roles throughout her career. Her passion for clinical research was ignited by her work as a research assistant and study coordinator, helping patients…

Lesley is currently the Associate Director of Product for IQVIA Technologies, Site and Planning Suite. She has over 15 years of industry experience with various perspectives, which she has gained from multiple roles throughout her career. Her passion for clinical research was ignited by her work as a research assistant and study coordinator, helping patients…

Dr. Lestter Cruz Serrano is the Head of Global Medical Affairs & Health Sciences Strategy in Cognizant, responsible for all 3 verticals – Healthcare, Life Sciences & Medical Devices – under the Cognizant Health Sciences division. He has been instrumental in driving adoption of Cognizant’s products & platforms, like, Shared Investigator Platform (SIP)—the industry’s first…

Dr. Linda Pao, MD, FAAN is a board-certified neurologist and clinical researcher dedicated to advancing therapies for neurodegenerative diseases. She serves as Co-Medical Director and Principal Investigator at JEM Research Institute, where she leads clinical trials focused on disease-modifying therapies for Alzheimer’s disease, Parkinson’s disease, Lewy Body Dementia, and related disorders. Dr. Pao’s approach to…

A Senior Site Operations Manager with over a decade of research experience, research is my passion. When I first started in the clinical research world I was unsure, but quickly realized this was what I was made for. Working to offer research as a care option all while expanding the future of medicine is something…

Lindsey Morales has worked in the clinical research industry for the last 18 years at sponsors, CROs and research sites. Her background includes roles in site relationship management, site identification, feasibility, study start-up and site monitoring. She currently serves as an Associate Director in Clinical Site Partners at Gilead Sciences. Lindsey holds a Bachelor’s degree…

Lisa has been involved in clinical research for over 25 years. She has directed both early and late phase research sites,and has experience in both project management and business development. Having worn many hats in her career, she brings a unique perspective to drug development.

Lisa has been involved in clinical research for over 25 years. She has directed both early and late phase research sites, and has experience in both project management and business development. Having worn many hats in her career, she brings a unique perspective to drug development.

With over 25 years of experience in healthcare and clinical research, Lisa is a results-driven executive recognized for leading high-impact initiatives across clinical operations, project management, strategic planning, and business development. Her career spans global leadership roles within top-tier organizations, including Fortrea, Labcorp Drug Development, Syneos Health, and PPD, where she has overseen clinical programs…

Lisa Malak is a seasoned healthcare leader, currently serving as a Director of Operations at Tandem Clinical Research. With a dynamic career spanning clinical care, operational strategy, and research, Lisa brings a unique, multidimensional perspective to leadership and workforce engagement in healthcare settings. Lisa is deeply passionate about clinical research, recognizing its vital role in…

Lisa Sonneborn, President of Ichor Research, began her career in clinical trials over a decade ago. Starting her career at a premier clinical trial site in Florida, Lisa explored as many roles as was possible before she independently founded and oversaw the growth of her first stand-alone clinical trial facility in Upstate NY, a dedicated…

With 15 years of experience in clinical research, I started my career as a research assistant and gained expertise across various roles in the industry. My passion lies in advancing clinical drugs through the phases of development to FDA approval, knowing my work contributes to improving lives. I loved working directly with patients, but discovered…

Lori Rich brings over 16 years of experience in accounting and finance. As VP of Financial Operations for the Financial Management Services division of Elligo she is responsible for the operations and growth of the network of research institutions within the service line. Prior to joining Elligo she worked as VP of Financial Operations for…

Lourdes López Bravo is an AVP, Clinical Operations and Head of Global Clinical Trial Operations for the European Economic Area (EEA) at MSD, based in Madrid. With more than 25 years of experience in clinical research, Lourdes leads the delivery of complex, multinational clinical trial portfolios across Europe, working closely with investigative sites, regulators, and…

Dr. Lovie Negrin, CEO of Randomize Now, works to involve marginalized communities in clinical trials, implementing strategies to educate and offer advanced treatments with the goal to reduce healthcare disparities. She is also a co-founder of the Noir Research Collective, a membership SMO.

Lucia is the founder and Director of Research for Evolve Clinical Research, a diverse multi-site network of sites in Arizona. She has worked in the field for over a decade playing multiple key roles at the site level for over and as consultant for academic centers and pharmaceutical companies. In her current role, Lucia oversees…

CEO – Medical Director of IBPCLIN Instituto Brasil de Pesquisa Clínica – MD PhD, MBA and BCMAS (Board Certified Medical Affairs Specialist).- Clinic Manager and responsible for Clinic Research expansion in Brazil. IBPCLIN is a Clinical Trial Center , dedicated to conduct multicentric clinical trial for pharmaceutical industries. Experient staff conducting studies with new investigative…

Luke Snedaker is a seasoned clinical research professional and CEO of West Clinical Research, Inc., an independent research site based in Morehead City, North Carolina. With a strong background in clinical site operations, site management, and regulatory compliance, Luke has built a reputation for leading high-quality, patient-centered clinical trials across multiple therapeutic areas, including Endocrinology,…

Mackenzie McKinney is Executive Director, Site Solutions and Patient Experience at Jumo Health. She leads strategic initiatives that deliver high quality patient and caregiver education at the moment of need and simplify site training and engagement. At Moderna she integrated patient voice with technology and services, including home health, travel concierge, participant payments, and digital…

Mackenzie McKinney has spent much of her career dedicated to reducing friction in clinical trials. She specializes in translating site and patient insights into high-impact digital solutions that drive recruitment, enrollment, and retention. Currently the Executive Director of Product at Jumo Health, Mackenzie leads the development of a platform designed to govern trial readiness by…

Madeline Sims is a Site Alliance Manager with over 11 years’ experience in clinical research across Phase I–IV studies. Madeline leads alliance‑site performance and strategy at Parexel, focusing on strengthening site partnerships, enhancing feasibility and start‑up readiness, and improving visibility of site capabilities. Madeline brings practical expertise in helping sites identify and position themselves for…

Dr Mahadev Ramjee is the Chief Medical Officer for Panthera Biopartners. He is a GMC(UK) registered physician with a background in Stroke and Geriatric Medicine and is a Member of the Royal College of Physicians. He has clinical research experience as Principal Investigator and Chief Investigator across a number of therapeutic areas within General Internal…

Marc brings more than 17 years of product leadership experience across healthcare, life sciences, and software. He most recently served as senior vice president of enterprise product management at Myriad Genetics, where he built and led a 40-person team and co-managed a multi-business unit P&L. He has also held senior product roles at Florence Healthcare,…

As the VP of Compliance & Security, Marc is leading the corporate security, quality and compliance initiatives at CRIO. Additionally, he’s serving as CRIO’s Data Protection Officer. Prior to CRIO, Marc was leading the Quality Assurance efforts at snapIoT.. Before snapIoT, Marc was a key member of the Corporate Compliance and QA group at Clinical…

Marcy Kravet is an experienced executive with over 25 years of leadership in the clinical trial industry, driving innovation and operational excellence. She started her research career as Director of Operations for a multi-site primary care research network. Marcy then moved to the sponsor side where she held key Clinical Operations leadership roles at Bristol…

Dr Maria Koufali is the Life Sciences Industry Director at the National Institute for Health and Care Research (NIHR), and formerly led the UK Vaccine Innovation Pathway as Head of the programme. Maria Koufali, is an experienced senior leader in life sciences research and innovation, bringing over 20 years of cross-sector expertise in working with…

Dr. Maria Ximena Graber is the CEO at AGA CLINICAL TRIALS since 2007 (USA / ECUADOR), a Clinical Research professional, Alliance Board Member, and Vice-President at HyperCore International. Dr. Graber is a dedicated medical professional with a diverse background and triple certification as a Certified Research Professional (CPI, CCRP and QM-IAOCR). Her expertise extends not…

Dr. Maria Ximena Graber is the CEO at AGA CLINICAL TRIALS since 2007 (USA / ECUADOR), a Clinical Research professional, Alliance Board Member, and Vice-President at HyperCore International. Dr. Graber is a dedicated medical professional with a diverse background and triple certification as a Certified Research Professional (CPI, CCRP and QM-IAOCR). Her expertise extends not…

Dr. Marianne Saurenmann is Director, Regional Lead, Study Site Engagement at Takeda. She and her team partner with clinical research sites to accelerate study start up, strengthen sponsor–site collaboration, and support reliable patient enrollment across Europe. With 25 years of experience in the pharmaceutical industry and CROs, Marianne has held roles across Clinical Operations, Medical…

Mariel Peitiado is a pharmacist who graduated in 1993 from the Universidad de Buenos Aires in Buenos Aires, Argentina. She has 30 years of experience in the pharmaceutical industry and extensive expertise in clinical trials. She is currently based in Argentina. She began her career in the pharmaceutical industry, and after working primarily in regulatory…

Clinical research professional with over 25 years of industry experience in trials across multiple therapeutic areas with extensive knowledge of study management, monitoring, vendor management and digital solutions. Dynamic leader skilled in agile development and innovation with a track record of successful implementation of large-scale change programs and simplification projects. Passionate about dismantling hierarchical silos…

Mark McKenzie, M.D. is the Chief Medical Officer responsible for strategies and new initiatives in the clinical and therapeutic areas. He also provides medical and clinical oversight to EmVenio’s team of principal investigators involved in trials at community research sites globally. Dr. McKenzie joined EmVenio Research in 2023 with more than 20 years of experience…

Dr. Weinberger oversees the strategic direction, expansion and day-to-day operations of the company. Under his leadership, IMA has experienced significant expansion in geography and service offering. Dr. Weinberger received his MS and PhD degrees in Clinical Psychology from the University of Massachusetts Amherst and his MPH in epidemiology from New York Medical College. In 2018,…

Over 30 years of global clinical research industry experience across all phases of drug development. Proven track record in providing strong leadership and operational excellence input, as well as therapeutic and business development insight to CRO and Sponsor partnerships.

Ms. Anderson serves as the Chief Business Officer (CBO) at Profound Research, a leading clinical trial site network. With over 30 years of experience in the clinical trial industry, Marty has been instrumental in spearheading operations since the company’s inception. Prior to joining Profound Research, Marty held significant positions in the clinical research field across…

Mary Jane Verastigue is a Clinical Quality and Training Manager at Novo Nordisk Pharmaceuticals Pty Ltd, based in Sydney, with over 20 years of experience in clinical research, quality assurance, and training. In her current role, she leads clinical quality oversight and inspection readiness across the Oceania Clinical Development Centre, embedding quality‑by‑design principles across the…

I love change & taking the creative, unconventional approach to solving complex problems. I like to listen, I like to learn & I love to draw. Passionate about driving innovation and inclusivity in clinical research, I bring 15 years of experience spanning Quality Assurance, Patient Recruitment, Clinical Data Management, and Study Management. My journey in…

Mary Williams is Director, Head of Site Relationship Management for Merck Global Clinical Trial Operations US. In this role, she is dedicated to building strong site partnerships that help deliver the Merck portfolio and improve the site experience. Her team innovates and collaborates with clinical trial sites to accelerate timelines, reach more participants, and ensure…

Maryleen Lovell-Petronilia, MSc, is a Medical Biologist specialized in Molecular Pathology, with over 14 years of experience in clinical research and healthcare innovation. In 2022, following a 10-year tenure at a prominent University Medical Center, during which she introduced Risk Management into routine clinical Pathology, Maryleen assumed the role of Manager of Quality Assurance and…

Matt holds the ACRP-CP and CCRC certifications through ACRP and is a member of SCRS, ACRP, and SOCRA. He has over 16 years of experience in clinical research on both the site and sponsor levels. On the site side, Matt has worked as a study coordinator, site manager, and director of clinical research, and assists…

I am software engineer with over two decades of experience driving innovation in AI, data platforms, and healthcare. At Fortrea, I design and develop advanced machine learning and AI systems to help make clinical trails more successful. This includes using neural networks to model risk models, agentic data extraction and AI multimedia generation to simplify…

As a practising Clinical Pharmacist with 28 years of Pharmaceutical experience in both the retail and hospital sector, I have a primary focus in delivering professional, ethical and evidenced based quality use of medicines to promote health and wellbeing. A retail Pharmacy owner for 13 years with experience in relocating and refitting of various pharmacies,…

Mazhar Jaffry is the CEO of Revival Research Institute and has over 32 years of expertise in the healthcare field. He has been a valuable resource for the Clinical Research industry from its inception. Mazhar Jaffry has long been an outspoken supporter of patient-centered care. His trailblazing initiatives, novel therapeutic approaches, collaborative efforts, ethical practices,…

Megan Morrison is the Chief Executive Officer of Paratus Clinical, bringing more than 24 years of experience in the clinical research industry. She has held senior leadership roles across sponsor organisations, CROs and clinical sites, giving her uniquely comprehensive perspective on the challenges across the drug development ecosystem. With a background in pharmacology and a…

Melissa is the Head of Site Management and Monitoring (HSMM) and oversees key tasks related to site management, territory development and country study support. The Head of SMM is responsible for monitoring resource management, capacity assessments of Clinical Research Associate (CRA) workload and overall quality of monitoring deliverables. With 20 years of clinical research experience…

Melissa Harris is Global Head of Patient Recruitment, Engagement and Modelling at Fortrea, with more than 25 years’ experience accelerating representative recruitment across all phases of clinical research. She leads programmes that reduce study burden and integrate participation into everyday life, while advancing health literacy, diversity and inclusion, and patient access equity. Melissa’s personal passion,…

Michael J. Cohen, MSc, MBA, SEP, is the Senior Director, Lead, Environmental Sustainability for the PPDTMclinical research business at Thermo Fisher Scientific. He is part of the Environmental, Health & Safety leadership team, supporting environmental sustainability across various businesses, including clinical research, laboratories, clinical trial sites, and real-world evidence. His role involves developing environmental sustainability…

Mike began his career in clinical development over 25 years ago and has experience spanning Phase I through IV operations. He holds a Masters of Science in Pharmaceutical and Medical Device Law as well as a Bachelor’s of Science in Biology. Before Fortrea, Mike spent 15 years with a large, global CRO, beginning as a…

Michael Fites is a seasoned Senior Feasibility Strategist with over 20 years of experience in the pharmaceutical industry. His expertise lies in clinical trial optimization and strategic planning, where he has successfully leveraged data-driven insights to enhance study design, site selection, and resource allocation. Michael has a proven track record in cross-functional leadership, fostering collaboration…

An Innovative Integrator with the goal to drive Access to enable Clinical Trials to be a Health Care option while reducing the burden on the patient & Investigator all while accelerating the development of medicines to those in need. Drug development expert with experience in: • Decentralized Trials leader • Taking the clinical trial to…

Michael Pierre is a Project Manager for SCRS and has been part of SCRS and the Summit program beginning with the first Summit held in New Mexico in 2006. He brings 18 years of experience in negotiating clinical trial agreements and budgets between sites and sponsors/CROs, including budget build and site contract support for phase…

Michael Pierre is a Project Manager for SCRS and has been part of SCRS and the Summit program beginning with the first Summit held in New Mexico in 2006. He brings 18 years of experience in negotiating clinical trial agreements and budgets between sites and sponsors/CROs, including budget build and site contract support for phase…

Michael Pierre is a Project Manager for SCRS and has been part of SCRS and the Summit program beginning with the first Summit held in New Mexico in 2006. He brings 18 years of experience in negotiating clinical trial agreements and budgets between sites and sponsors/CROs, including budget build and site contract support for phase…

Michael Pierre is a Project Manager for SCRS and has been part of SCRS and the Summit program beginning with the first Summit held in New Mexico in 2006. He brings 18 years of experience in negotiating clinical trial agreements and budgets between sites and sponsors/CROs, including budget build and site contract support for phase…

Michael Pierre is a Project Manager for SCRS and has been part of SCRS and the Summit program beginning with the first Summit held in New Mexico in 2006. He brings 18 years of experience in negotiating clinical trial agreements and budgets between sites and sponsors/CROs, including budget build and site contract support for phase…

Mike Watson brings over 16 years of experience in ophthalmology clinical research, spanning clinical operations, site development, and business development. He currently serves as Vice President of Therapeutic Development at Ora, where he previously built and led the company’s strategic Ophthalmic Site Network and Patient Solutions department. There, he encouraged his team to listen closely…

I am a chemical engineer by education with additional masters in public health. With 18+years experience in clinical research – as CRA, sCRA, PM, SC, Site Director – at Sponsor companies, CROs, site network and Vendor. Recently, I have joined Global Clinical Trials, as Business Development Director. GCT is a Contract Research organization operating in…

Michele Cameron is the Director of Clinical Research for Clearwater Cardiovascular Consultants (CCC), a large independent cardiology practice located in Clearwater, Florida. Michele joined the Dept. in 2005 and has since grown and cultivated a highly successful practice-embedded site. The Site conducts 30-35 cardiovascular related drug and device studies in both the clinic and hospital…

Michelle Hartmann, CCRP, is the Director/Owner of South Broward Re-search which is located in SE Florida. She started with South Broward Research in 2006. South Broward Research is a community based, inde-pendent site. She is dedicated to the pursuit of advancing healthcare by ensuring integrity and quality in the work performed at South Broward Research….

Michelle Hartmann, CCRP, is the Director of South Broward Research located in SE Florida. South Broward Research is a community based, independent site. She is dedicated to the pursuit of advancing healthcare by ensuring integrity and quality in the work performed at South Broward Research. She feels fortunate to be a part of an incredible…

Michelle Jones is a business development and operations executive with over 30 years of global leadership experience driving revenue growth through strategic planning, operational transformation, and brand development. She has a proven record of leading high-performing teams, launching successful business units, and delivering measurable results across clinical research and life sciences sectors. As Senior Vice…

Most people building technology for clinical research sites have never worked at one. I have — for over a decade, across roles that span the full reality of how sites actually operate. That background shapes everything about how I sell, what I build relationships around, and why customers tend to trust me faster than they…

Mike Stratton is a seasoned leader in the clinical research industry, known for driving innovation in global patient recruitment and retention. As President of CSSi, Mike has led the company through a transformative era—modernizing operations, expanding global capabilities, and introducing cutting-edge, site-first enrollment solutions that meet the complex needs of today’s trials. Prior to joining…

Dr. Mimi Fenton, CEO of Cedar Research and Aspen Insights, is an experienced Life Sciences executive with 20+ years of experience in Global Pharmaceuticals (Sanofi), Pharmaceutical Services (Syneos Health), Retail/Pharmacy (Walmart) and Academia (Columbia University, Rutgers University). Mimi has extensive experience developing innovative evidence generation strategies to unlock powerful drug and device value propositions across…

Iburahim is a Clinical Research Coordinator III at the University of Chicago Comprehensive Cancer Center, where he supports Phase I–III oncology trials with a focus on hematologic malignancies, cellular therapies and bone marrow transplant. He holds a medical degree and brings a strong clinical perspective to complex trial operations, playing a key role across both…

Driven by a deep commitment to patient care and innovation, Mohammad is an active contributor to the clinical research ecosystem, serving on multiple leadership committees and shaping industry-wide best practices. He was recognized as one of the Top 25 Healthcare Technology Leaders of Houston in 2023, reflecting both his strategic vision and his impact on…

Pharmacist with a strong foundation in clinical research, which began even before graduating from Federal University of Rio Grande do Sul (UFRGS). She started her professional career as a clinical research coordinator in oncology where she developed hands-on experience in clinical study conduction. Over the past two decades, she has transitioned into the pharmaceutical industry,…

Murray Aitken is head of the IQVIA Institute for Human Data Science, where he provides policy setters and decision-makers in the global health sector with evidence, analysis, and insights that contribute to the advancement of Human Data Science to improve human health outcomes. Throughout his nearly 25-year career at IQVIA, Murray has helped to address…

Dr My‑Nhan Nguyen is Deputy Director of Research at St Vincent’s Hospital Melbourne, where she supports the Director of Research in providing strategic and operational leadership across research governance, ethics, and research facilitation. Since joining St Vincent’s in 2021, she has held multiple roles across St Vincent’s Hospital Melbourne and St Vincent’s Health Australia, leading…

Nachiket Chandak is Chief Commercial Officer at FutureMeds, joining the Executive Leadership Team as sponsors and CROs push for faster, more predictable delivery. He focuses on strengthening how FutureMeds partners with clients by aligning feasibility, start-up planning and delivery governance early, reducing avoidable friction once studies are underway. Nach brings 18+ years’ experience in clinical…

Nadir Ammour is a Global Lead for External Engagement at Sanofi, a global healthcare leader dedicated to chasing the miracles of science to improve people’s lives. In this role, Nadir manages and coordinates external engagement initiatives within the Engagement & Strategic Collaborations function in clinical operations. Nadir graduated as a medical dentist and holds an…

Nancy Dicristo is a seasoned life sciences executive with experience spanning operational and commercial leadership roles. She began her career on the sponsor side at Schering Plough and Celgene Corporation, supporting global clinical trials through commercialization. This foundation shaped her expertise in protocol feasibility, programmatic and site level budgeting, and forecasting complexity at scale. Nancy…

Over 20 years’ experience in the pharmaceutical industry with progressive roles in clinical operations. Since 2022, post-implementation of the EU Clinical Trials Regulation (EUCTR), I have headed the Regional Submission Leads team for all EEA countries, overseeing and executing all EU clinical trial submissions through the Clinical Trial Information System (CTIS).

Natalie Robertson is the Senior Manager of Strategic Partnerships at Tribe Clinical Research, where she leads initiatives focused on cross-functional collaboration, strategic growth, and relationship building. Since Tribe’s formation in 2020, Natalie has played a key role in the company’s development, contributing to systems design, operational alignment, and meaningful partnerships that support long-term success. With…

I am a strategic partnerships and business development leader focused on improving how clinical research reaches and supports patients. I currently serve as Senior Director of Strategic Partnerships and Business Development at Civia Health. I was drawn to Civia because of its clear focus on both the patient experience and how research is delivered. The…

Neil Sheth serves as Director of Medical Operations, US at Accelerated Enrollment Solutions within the clinical research business of Thermo Fisher Scientific. Dr. Sheth is Board Certified in Family Medicine and Lipidology and has over 10 years of PI experience.

Nelly joined Parexel in May of 2021 as the Chief Information Security Officer. Nelly brings over 24 years of leadership experience in managing Cyber risks and developing robust Cybersecurity programs. Prior to joining Parexel, Nelly was deputy CISO/Managing Director at Moody’s. Nelly has extensive experience in building Information Security Programs, implementing defenses based on best…

Nelly Nauman joined Parexel as Chief Information Security Officer in May 2021, bringing over two decades of leadership experience in cybersecurity and risk management. In her role as CISO, Nelly leverages her extensive background to develop comprehensive Cyber Security Programs and robust defense strategies, ensuring the protection of critical assets and information in an evolving…

Nicholas Focil is the founder and CEO of FOMAT Medical Research– an Integrated Research Organization with over 10 years of experience conducting clinical research in a wide variety of therapeutic areas. As CEO of a medical research company, Nicholas aims to diversify clinical trials, bring innovative healthcare to underrepresented populations, and ensure that high-quality data…

Nicholas Focil is the founder and CEO of FOMAT Medical Research– an Integrated Research Organization with over 10 years of experience conducting clinical research in a wide variety of therapeutic areas. As CEO of a medical research company, Nicholas aims to diversify clinical trials, bring innovative healthcare to underrepresented populations, and ensure that high-quality data…

Dr Nick Probert is a Fellow of the Faculty of Pharmaceutical Medicine in the UK. He has worked in clinical research sites for the last 12 years and led medical departments in health-tech and small pharma companies. He is a registered specialist in Pharmaceutical Medicine, previously training as surgeon in the NHS. He has contributed…

Nicole founded Meridian Clinical Research in 1999 in Omaha, NE, with a fax machine and a credit card advance. She grew Meridian from a single location to a network that included more than 30 brick-and-mortar sites and 90 physicians across North America, enrolling more than 40,000 patients across 2,400 clinical trials. Under Nikki’s direction, the…

Nicole is the CEO of Todata Analytics, where she is focused on helping clinical research sites turn the data they already have into clear, actionable insights, without adding complexity to their day-to-day operations. Before Todata, Nicole was the founder of Meridian Clinical Research, one of the largest clinical research site networks in the country. Having…

Nikita Zubkov is a Digital Marketing Growth Manager with a strong focus on social media–driven patient recruitment for clinical trials. In his role, he develops and scales online campaigns that connect study sites with eligible patients through data-driven digital channels. With hands-on experience in planning, executing, and optimizing paid social media campaigns, Nikita specializes in…

Experienced Clinical Research professional with over 20 years in the industry, currently in the position of Innovation Lead for South Cone at Sanofi. Her career spans key roles including Study Coordinator, Clinical Research Associate, Clinical Lead, and Local Study Manager. She is skilled in leading multidisciplinary teams, enhancing digital capabilities, and driving operational efficiency. In…

Professional with a degree in Medicine with experience developed in Pharmaceutical Companies as Medical Advisor and CRA. Teaching skills focusing on Pharmacology and Therapeutic areas. Attendance and participation in international meetings. Author of publications in scientific papers. Fluent oral and written English and knowledge of PC. Analytic with strong leadership skills, as well as decision…

Oshrat Goldberg is the Chief Commercial Officer at Mural Health, a clinical trials technology company dedicated to making it easier to participate in clinical trials. Leveraging her experience driving strategy and execution in various healthcare and life sciences organizations, Oshrat leads Mural Health’s work to drive business growth by creating patient-centric solutions in clinical trials….

Pam Ramali is the CEO of Clinibase, Australia’s largest and fastest-growing full-service patient recruitment and clinical trial technology company. Headquartered in Melbourne, Clinibase has recruited for 200+ trials across 40+ indications in partnership with 50+ sites throughout ANZ. Its proprietary CTMS and eSource technology powers sites, Sponsors, and CROs with real-time data. Pam’s career spans…

Patricia Peters is currently assigned to the Operational Excellence Lead for MSD ANZ, partnering with GCTO ANZ leadership to strengthen Clinical Site Partnerships, onboarding and engagement, resource management, and performance analytics. She is accountable for aligning resources across Australia and New Zealand, ensuring portfolio assignments are efficient and effective to maximise productivity and quality. Patricia…

Paul is the Business Developer at Dr. SOM (Segunda Opinión Medica) and AveSalud, sites located in Barranquilla and Cartagena, Colombia. He is a Dental Surgeon from Universidad San Martín de Porres, Peru, and holds an MBA in Strategic Business Administration from Pontificia Universidad Católica del Perú (PUCP). Throughout his 25-year career in clinical research, Paul…

With over 20 years of global clinical research experience in the Biotech and CRO fields, Paula specialises in accelerating clinical trial delivery, optimising recruitment, and fostering strong site partnerships to ensure high-quality, efficient trial execution. Passionate about site engagement and strategic collaboration, Paula works closely with key stakeholders across the clinical trial ecosystem to drive…

Paula is a seasoned leader with extensive global experience in driving strategic site collaborations and clinical engagement across the healthcare and life sciences sectors. Currently working as the Senior Director, Head of Strategic Site Collaborations, PPD, part of Thermo Fisher Scientific, responsible for steering strategy and transformational operational changes to ensure the success of the…

Paula is a seasoned leader with extensive global experience in driving strategic site collaborations and clinical engagement across the healthcare and life sciences sectors. Currently working as the Senior Director, Head of Strategic Site Collaborations, PPD, part of Thermo Fisher Scientific, responsible for steering strategy and transformational operational changes to ensure the success of the…

Paula is a seasoned leader with extensive global experience in driving strategic site collaborations and clinical engagement across the healthcare and life sciences sectors. Currently working as the Senior Director, Head of Strategic Site Collaborations, PPD, part of Thermo Fisher Scientific, responsible for steering strategy and transformational operational changes to ensure the success of the…

Piotr Sawicki – Graduate and lecturer at the Kozminski University. He has been associated with the clinical trials market since the late 1990s, dealing with the activities of Research Sites and patient recruitment and retention. Co-founder of the Osteomed Medical Center and the Clinical Research Center ( Phase I unit) An expert in Site Management,…

Priya Selvarajah, MD, serves as Regional Site Director at IMA Clinical Research, overseeing clinical operations across a network of high-performing research sites. With a background in medicine and over 10 years of experience in clinical research, she brings a strong foundation in clinical understanding paired with strategic site leadership.

Rachana Kanvinde is a certified clinical research leader with over two decades of experience in clinical operations, research methodology, and site network management, with a strong focus on rare disease research. She currently serves as Director of Clinical Site Network Operations at Rare Disease Research, where she leads strategic initiatives to optimize clinical trial efficiency,…

Rachel brings nearly 30 years of clinical research experience to the panel. She has held a wide range of roles across the industry including Study Coordinator, Clinical Research Associate, Project Manager, Clinical Team Leader, and Executive Leader in both academic and contract research organization (CRO) settings. Leadership roles began at MD Anderson Cancer Center and…

Rachel has worked across various areas of the clinical research industry including in a site network, a CRO, and currently at a sponsor company, as the Director of Site Planning & Optimization for Boehringer Ingelheim. In her current role, she is part of the Clinical Development and Operations Leadership team, leading a group focused on…

Radhika is a passionate Clinical Researcher and Site Advocate with over 20 years of experience and expertise from Trial Coordination to Trial Unit establishment. She has diverse clinical trial expertise in interventional and device studies spread across multiple therapeutic areas. She has operational and managerial experience in the public, private, commercial and academic sectors within…

CEO of Irvine Clinical Research, the largest independent site network on the US West Coast, as measured by clinical trial payments. Irvine has four sites in Greater Los Angeles area with diverse doctors, staff, and study participants. Irvine’s research is focused in Neurology, and also has specialists in Psychiatry and Obesity.

Futurist, author, and former Head of Innovation at Mattel, Ramy Nassar helps leaders navigate AI and emerging technology with confidence. His presentations cut through the hype with bold foresight and practical tools—leaving audiences energized, inspired, and ready to Navigate What’s Next—accelerating innovation, reimagining strategy, and shaping the future before it disrupts them.

I’m Ravi Alla, Director of Clinical Administration at Revival Research Institute. I oversee day-to-day operations across multiple clinical research sites, working closely with our teams to ensure high-quality execution, regulatory compliance, and strong performance metrics. My focus is on streamlining processes, improving site efficiencies, and leading key initiatives from site expansion and system implementation to…

Raymond Nomizu is the co-founder and co-CEO of CRIO, an e-clinical provider for sponsors, CROs and sites. CRIO’s system allows research sites to collect data accurately and contemporaneously, and sponsors to view the data in real-time, without costly source data verification. Prior to founding CRIO, Raymond owned and operated an independent clinical research site; co-founded…

Dr. Rebecca Goldfaden currently holds the position of Chief Scientific Officer and Head of Business Development for Rovia Clinical Research, a site network company. She holds a Doctorate of Pharmacy from the University of Florida and completed a PGY-1 Pharmacy Residency focused on cardiology and endocrinology. Dr. Goldfaden also completed a Post-Doctoral Fellowship in Clinical…

Rebecca Cargill is a senior clinical operations leader with over 20 years of experience delivering complex clinical trials and cross functional programs across Australia, New Zealand, and the Asia Pacific region. She is currently Senior Manager, Clinical Operations at Johnson & Johnson, where she is accountable for successful country execution of clinical trials, including resourcing,…

Rebecca is the head of IQVIA’s Site Enablement Solutions team, a service offering within IQVIA’s Patient & Site Centric Solutions team that supports sites to increase their potential by providing research-experienced staff to support clinical trial protocols. Rebecca has 15 years of experience working within CROs, with her experience focused on site engagement and support…

Renata is a Senior Director of Clinical Research Informatics and Technology at Memorial Sloan Kettering Cancer Center, where she leads a specialized team of technologists supporting global clinical trials through digital health and IT solutions. With over 15 years of experience in oncology research, she is a seasoned innovator, recognized for advancing technologies that enhance…

Dr Nally has been a GP Partner at Wansford Surgery for 30 years, stepping down in September 2024. A Fellow of the Royal College of General Practitioners, she was a GP Trainer for 22 years and spent many years as Older People’s Lead for Cambridgeshire, developing Multidisciplinary Team Working across Primary and Secondary Care, Community…

Hey, I’m Rhys! I’m a Senior Clinical Trial Coordinator at Emeritus Research with close to four years of experience working across Phase I to III clinical trials in a wide range of therapeutic areas. Most of my experience has been in gout and Alzheimer’s trials, where working closely with vulnerable patients has really highlighted the…

Rick has over 20 years of experience in the Clinical Research industry. He was part owner and helped build one of the largest multi-specialty research sites in the US over a 13 year period. With a lack of truly effective and efficient CTMS systems available, he put his education in Information Systems to work and…

As Chief Commercial Officer at CRIO I am responsible for driving commercial growth strategies, increasing existing market penetration, and maximizing expansion into new markets. I lead an increasingly impressive team of professionals dedicated to improving clinical research execution via CRIO’s best-in-class eClinical solutions. A proven leader in driving commercial growth strategies at dynamic eClinical solution…

Rick has almost 25 years of clinical research experience ranging from site ownership and operations to eClinical software development and worldwide deployment. Rick is passionate about improving industry workflows and efficiencies with a focus on site health and patient advocacy through meaningful partnerships and technology.

Dr. Roberto Aguirre, VP, Founder, and Global Research Director of AGA Clinical Trials since 2007, stands at the forefront of clinical research leadership. His journey is a testament to unwavering commitment, innovation, and transformative impact. As one of AGA Clinical Trials’ original founders, Dr. Aguirre spearheaded strategic initiatives that transformed the organization into one of…

Robin joined Medidata Solutions in March 2024 as VP, Research Site Engagement and will be leading efforts for Medidata’s Site Insights Program. Her clinical research career spans over 30 years, with various leadership roles at investigator sites, IQVIA, Marken, and CVS Health. She has expertise in strategy, innovation, clinical operations, DCT implementation, site engagement and…

Experienced clinical research professional with solid life science background (PhD from National University of Singapore, visiting scholar at Harvard Medical School), currently working as Site Engagement Lead at Sanofi, and a leadership board member at the Clinical Trial Management Society – Hungary.

Roman Fishchuk is an adept ENT doctor with twelve solid years of practice experience. Ability to work in a multidisciplinary team, experience in delivering patient care in both public and private settings with the use of the latest industry equipment and technology, as well as establishing own private practice. Proactive and dedicated to seeking opportunities…

Roman Fishchuk is an adept ENT doctor with twelve solid years of practice experience. Ability to work in a multidisciplinary team, experience in delivering patient care in both public and private settings with the use of the latest industry equipment and technology, as well as establishing own private practice. Proactive and dedicated to seeking opportunities…

Roman Fishchuk is an adept ENT doctor with twelve solid years of practice experience. Ability to work in a multidisciplinary team, experience in delivering patient care in both public and private settings with the use of the latest industry equipment and technology, as well as establishing own private practice. Proactive and dedicated to seeking opportunities…

Roshan Yadama currently serves as Chief of Staff & VP of Corporate Strategy at Profound Research, where he also heads the company’s Data Governance initiatives. Profound is a best-in-class clinical research site network with studies in multiple therapeutic areas, dedicated to expanding access to clinical trials for all patients. Founded in 2023, Profound has 1200+…

Ruth Lucas is a clinical research professional with over 20 years of experience in the clinical trials industry. Beginning her career in the UK, Ruth conducted trials across all phases before relocating to New Zealand in 2006. Throughout her career, Ruth has worked with CROs, pharmaceutical companies, and healthcare organizations, with a strong focus on…

Samantha Prins is Director Business Development and Start-Up, supporting the acquisition, contracting and set-up of clinical trials along with her team. She is the first point of contact for potential clients wanting to work with Progress Clinical Research. Samantha has a PhD in neuroscience obtained during working at a dedicated phase 1 clinical trial unit….

Sara Brueck Nichols is the President of McCreadie Group, a leading provider of innovative software solutions that advance pharmacy research and education. With nearly 25 years of experience in strategy, operations, and technology, Sara brings a proven track record of driving growth, operational excellence, and transformative change. Before joining McCreadie Group in 2024, Sara served…

Sara is a Registered Nurse with over 30 years’ experience across clinical care, health policy and clinical research. She has worked in clinical trials for more than 20 years and has supported studies across Australia, New Zealand, South Korea and South-East Asia. Sara also brings lived experience as a clinical trial participant, offering valuable insight…

Sarah is a seasoned oncology strategist with over 20 years of experience in oncology drug development across all indications and phases. She has a proven track record of leading clinical operations, global project management, and portfolio oversight, with a focus on advancing innovative treatments to patients and their care families. Currently serving as the Therapeutic…

Sarah Howells is Director, Clinical Site Centricity, for Clinical Development Operations at AbbVie. Sarah is responsible for enhancing the experience of site staff and investigators who are working with AbbVie on clinical research studies. Previously, Sarah served as Director, Strategic Communications and Performance Analytics within Clinical Development Operations at AbbVie. Prior to joining AbbVie, Sarah…

Savine DaCosta is the Clinical Trial Diversity Site Lead at Biogen. Savine is a subject matter expert in community engagement, apparent and hidden disability advocacy. Her authentic, heartfelt approach has been impactful with underrepresented communities understanding of clinical research.

Scott Bannan is the New Zealand Clinical Research Director responsible for: ensuring clinical trials in NZ are delivered to the highest quality standards; maintaining and growing our relationships with NZ sites and Investigators; and, leading the MSD clinical trials team in New Zealand. Scott is also a member of the ANZ clinical trials core leadership…

Scott Palmese has been in the clinical research industry for over 15 years and is currently Executive Director, Site-Focused Solutions at Worldwide Clinical Trials. In his role, he works with research sites across the globe to improve operations and find better ways to collaborate on new clinical studies. Prior to his time at Worldwide, Scott…

Scott Reid Rosen is a seasoned operations and growth specialist with over 15 years of experience spanning pharmaceutical research, start-ups, and consulting. As Co-Founder of Cortex Clinical Solutions, he drives innovation and operational excellence in clinical research, drawing on his proven track record as a founding member of the Alliance for Multispecialty Research, where he…

Scott Sumner has over 25 years in the field of Compliance and Information Security, and has been Chief Information Security Officer at a number of famous brands, including Godiva Chocolatier, Pepperidge Farm, Direct Brands and Tory Burch. His career has been spent helping organizations make transitions through times of change. This includes acquisitions, spinoffs, startups…

Sean Cunningham is a Study Site Engagement Regional Director (Americas) with Takeda Pharmaceuticals. In this role, Sean is dedicated to establishing, developing, and leveraging meaningful sponsor relationships to help accelerate the Takeda portfolio and provide sites with a positive clinical trial experience. Sean provides leadership and support for the activities of the Study Site Engagement…

Sean oversees the business development and operations for industry partnerships at the Society for Clinical Research Sites, and helped to launch SCRS with Founder, Christine Pierre. With a deep experience in association and publishing, Sean provides consultation, strategy and collaboration opportunities to the SCRS audiences, including: industry solution providers, pharmaceutical companies, contract research organizations and…

Sean oversees the business development and operations for industry partnerships at the Society for Clinical Research Sites, and helped to launch SCRS with Founder, Christine Pierre. With a deep experience in association and publishing, Sean provides consultation, strategy and collaboration opportunities to the SCRS audiences, including: industry solution providers, pharmaceutical companies, contract research organizations and…

Sean Stanton has spent the past 28 years at the forefront of clinical research site development, creating and leading high-performing research organizations dedicated to improving public health through innovation. As co-founder of K2 Medical Research, Sean leads a team of dedicated researchers focused on connecting groundbreaking clinical solutions with the health challenges facing communities today….

Shanna Nixon is a seasoned industry professional with over 26 years of experience at both the CRO and Clinical Research Site. Highly experienced in building strategic site partnerships. A team-oriented director who has demonstrated attention to detail, fiscal responsibility and completion of tasks with a sense of urgency as required by the timelines and milestones…

Shannon Zimmerman is an accomplished clinical research leader with over a decade of experience driving the success of complex clinical trials and advancing global research operations. As Senior Director of SiteChoice® Strategy and Execution at Transformative Pharmaceutical Solutions, she has been instrumental in scaling clinical site support across 22 countries, fostering seamless collaboration between sponsors…

Shelby Petereit is a Clinical Research Supervisor at Avera Research Institute in Sioux Falls, South Dakota. Shelby has a bachelor’s degree in business administration and a master’s degree in health sciences from Montana State University. Shelby leads study intake and study start-up for her team. She works alongside a leadership team who has a passion…

Established in 2010, Biopharma Informatic is an Investigator-led Clinical Research Network, intentionally expanding its research portfolio and global footprint. Central to our success is the exceptional leadership and mentorship provided by our physicians, whose expertise ensures the importance of our endeavors. Thanks to the steadfast dedication of our Principal Investigators and team, we have successfully…

Silvina Baudino is a site advocate with more than two decades of experience in the clinical trial industry. Commencing her career as a clinical research coordinator at a site in Argentina, she swiftly transitioned to various roles in clinical operations, feasibility and project management, garnering regional and global responsibilities. Her trajectory led her to the…

Silvina Baudino is a site advocate with more than two decades of experience in the clinical trials industry. Commencing her career as a clinical research coordinator at a site in Argentina, she swiftly transitioned to various roles in clinical operations, feasibility, and project management, garnering regional and global responsibilities. Her trajectory led her to the…

Silvina Baudino is a site advocate with more than two decades of experience in the clinical trials industry. Commencing her career as a clinical research coordinator at a site in Argentina, she swiftly transitioned to various roles in clinical operations, feasibility, and project management, garnering regional and global responsibilities. Her trajectory led her to the…

Simonne Breemans is an Associate Director of Clinical Operations at PPD, part of Thermo Fisher Scientific, with over 30 years of experience in clinical research. She began her career at the University Hospital of Leuven and subsequently worked as a Clinical Research Associate and within a sponsor organization before joining the CRO sector. Simonne has…

Sobia Dean is a Clinical Site Operations Manager with over seven years of experience in clinical research. She has worked across public hospitals, academic research, and the CRO environment, bringing a well rounded perspective to the complexities of clinical trial delivery. Throughout her career, she has managed studies spanning multiple phases and therapeutic areas, building…

Dr Reiter is a Partner at Lakeside Healthcare Research and a UK board-certified General Practitioner. She is an experienced Principal Investigator with a strong track record delivering both academic and commercial studies across multiple therapeutic areas. She is currently serving as the Primary Care Settings Lead for the NIHR RRDN East of England, co-chair of…

Spencer Jones brings extensive leadership experience across banking, fintech, and healthtech industries. As Senior Vice President of Trial Solution Products at Signant Health, he focuses on solving critical challenges that pharmaceutical companies face when bringing innovative therapies to market. Previously, Spencer served as Head of US Digital for TD Bank, the sixth-largest bank in North…

Stace Baumgarten began her career in Clinical Research Finance in 2005 and, over the past 20 years, has enjoyed working for Concentrics Research, Coastal Carolina Research Center, Alcanza Clinical Research, and Clinical Research Billing. Stace has managed A/R in Clinical Conductor, RealTime, and CRIO. She has been directly involved in policy development, training, billing, collections,…

Stacey Bledsoe, RN, MSN, Head of Clinical Patient Engagement and Inclusion, joined Gilead Sciences in July 2023 as Head of Global Clinical Trial Diversity and Inclusion. Her role has since expanded to include Patient Engagement, where she leads efforts to integrate the patient voice across the drug development lifecycle. She is responsible for advancing clinical…

Stacie Merritt currently serves as the Director of the Ascension St. John Clinical Research Institute in Tulsa, OK. She earned a Master’s in the Science of Nursing from the University of Oklahoma. Mrs. Merritt is recognized as a board-certified Clinical Research Nurse. Throughout her career, she has participated as a Primary Investigator and Sub-investigator in…

Stacy has spent 25+ years in healthcare and bridges the industry/consumer gap as a stage IV cancer survivor and 24/7 caregiver to her son with a rare disease. Her unique professional and personal experience position her as an esteemed global patient advocate as well as an influential pioneer in patient engagement. In her role as…

Experienced Director and Global program manager with a demonstrated history in global people leading, process innovation, contracts and budget negotiations, data analytics, Service-Level Agreements (SLA), ITIL, and project management. Strong business professional with a Bachelor of Science (BS) focused in Business Administration and Management, from Indiana University.

Stephanie Ailey is a highly accomplished industry veteran with over 20 years of experience in program management and healthcare. As the Vice President of Business Development at DM Clinical, she brings invaluable expertise to the national clinical trial site network. Her exceptional track record in building strategic relationships has been instrumental in driving the company’s…

Stephen is the Founder and Principal of Boeson Research, a clinical research company with Montana locations in Missoula, Kalispell, Great Falls and Bozeman; and Utah locations in Provo and Salt Lake City. Boeson Research focuses on phase 2-4 research projects in women’s health, pediatrics, family medicine, vaccines, dermatology, cardiology, psychiatry and mental/emotional health. Stephen earned…

Steve brings deep expertise in both healthcare and clinical research to his role as CEO of ObjectiveHealth. An experienced executive in the clinical trial space, he has founded, bought and sold multiple research entities, including VitaLink Research, which he guided to highly profitable growth as well as international expansion. Steve comes to ObjectiveHealth from Rymedi,…

Steve Satek has more than 35 years of experience in the research industry, starting as a bench researcher at the Northwestern University Robert H. Lurie Cancer Center through senior leadership positions at the Chicago Center for Clinical Research, Radiant Research, Cognitive Drug Research, and Forenap Pharma. In 2013, Steve founded Great Lakes Clinical Trials, a…

Industrial Engineer with one full year of MBA studies. Experienced and proven sales manager with 21+ years experience in the International logistics, freight management sector. Developed and implemented strategic business plans in different roles across 3 continents, South America, North America and Europe, which have resulted in increased adaptability and flexibility to varying challenges and…

Storm Stillman is the CEO of Sitebase, by Curebase. After years operating Curebase’s own CRO, virtual site, and full DCT services, he brings a deep understanding of what patients and sites truly need from technology, which is insight that now drives the vision behind building the company’s eClinical platform for sites. An operator at heart,…

Stuart Young has over 15 years of industry experience gained through multiple roles. In 2019, Stuart became the founding CEO of Panthera Biopartners, now one of the UK’s leading Site Management Organisation (SMO). Panthera operates seven large sites, deeply embedded in local healthcare and communities with a growing international presence. Panthera recruits thousands of patients…

Sue-Ann is the Study Start-up and Systems Manager for the Ramsay Research and Development Network. She leads a team focused on improving and streamlining clinical trial start-up processes across more than 20 clinical trial units embedded in Ramsay Health Care facilities. With experience spanning the full research lifecycle, Sue Ann brings practical knowledge of protocol…

Susan Johnson is a senior clinical operations executive known for transforming global research organizations, strengthening strategic partnerships, and delivering consistent operational and financial performance across complex, multinational portfolios. With more than 30 years of clinical experience spanning biotech, pharma, and CRO environments, she brings a rare combination of operational rigor, commercial acumen, and people‑centric leadership….

As the Director of Business Development and Strategic Marketing at AMR Clinical, I leverage 25+ years of clinical trial industry experience to create and execute strategic plans and partnerships that deliver quantifiable outcomes for internal and external stakeholders. I am accomplished at identifying and closing new opportunities, building and nurturing positive, long-term relationships with client…

Susan Hernandez, Director of Clinical Affairs at M3 Wake Research, is a distinguished healthcare leader with a proven track record in leading investigator engagement, optimizing operations, and driving business growth in the clinical trial industry. Her expertise extends from preclinical and formulation work as a pharmaceutical chemist, emergency department clinician, as well as investigator in…

Susan Tio has a background in Biomedical Science and a PhD in medical pharmacology from the Leiden University in The Netherlands. Part of the research for her PhD thesis was performed at the Rockefeller University in New York, USA. Over the past 30 years Susan has worked for various pharmaceutical companies varying from small to…

Suvi is the CEO and Co-founder of Monroe Biomedical Research, a leading and rapidly growing clinical trial site network specializing in multi-therapeutic studies. With more than 15 years of experience in the clinical research industry, Suvi has overseen Monroe’s growth into a high-performing organization recognized for its quality-driven patient enrollment and operational excellence. Under her…

Dr Suzanne Elliott joined Queensland Health at Metro North in September 2025 as Clinical Trial Business Development Manager. She began her career in Medical Laboratory Science across private and public pathology laboratories before moving into academia at QUT, focusing on molecular oncology. Her work helped establish the Mater Hospital molecular laboratory and contributed to vaccine…

With over 25 years of experience in the clinical research industry, I have dedicated 19 years as a Site Director at a private research clinic, where I successfully oversaw the completion of more than 150 clinical trials across 50 indications. Currently, I serve as a Site Relationship Manager, where I support both seasoned and novice…

Clinical Research Professional with 20+ years industry experience, with a proven record of driving successful clinical trial strategy and execution within a Biotech, CRO and Clinical Trial Site.

Tegan Roberts is the ANZ Feasibility Lead at IQVIA, with over six years’ experience working across CRO roles in study start‑up, site activation and feasibility. She began her career in hospitals and universities, working in clinical research across trauma, intensive care and cardiothoracic surgery, alongside teaching roles within university settings. She briefly spent time as…

Spanning over several decades as both a Registered Nurse and leader in Clinical Research, Theresa strives to prioritize both quality and excellence at the site level. The business of research has matured through the years, but the reasons we do it have not. Theresa has developed the personal approach to building a research site, gaining…

With over 25 years of trial operations experience in the clinical research industry, Tiffany McGinnis is a seasoned leader recognized for her ability to bridge the gap between complex operational requirements and meaningful human engagement. Her career is defined by a deep-rooted commitment to optimizing site management operations, a field in which she has spent…

Ting Yu, PhD, is the Systems Manager at Griffith University Clinical Trials Unit, where Ting leads the implementation, optimisation, and governance of core clinical trial technologies, including CTMS, electronic investigator site files system, and eSource platforms. With over 10 years of academic research experience in molecular microbiology and more than 4 years coordinating and delivering…

Todd Albin has nearly 30 years of experience in clinical research operations, with a focus on site management, patient recruitment, and expanding trial access to underserved populations. He currently serves as Director of Clinical Research at Insight Hospital & Medical Center in Chicago. His career spans leadership roles across site networks, CROs, and solution providers,…

Tom is the CEO and Co-founder of Delfa. Delfa builds an AI-native CRM for clinical research sites; helping them to be 5-7x more productive when recruiting participants. Previously he deployed global AI programs in partnership with companies such as J&J, Medtronic and Exscientia.

Tony Pearson is responsible for Lilly’s global commitment to increase clinical trial diversity, leading a team orchestrated to shape internal operations and evolve public policy while strategically engaging investigators and communities to reach representative patient populations across the globe.

Senior Director, Trial Capabilities, North America Tonya Edison joined Eli Lilly and Company in 2003 and has since held a variety of positions in support of patient safety, quality, and the delivery of clinical programs. Tonya currently leads the Trial Capabilities organization responsible for defining and executing strategies for site activation, maintenance, execution of clinical…

Trisha Gordon is a seasoned leader in clinical operations with nearly two decades of experience driving efficiency and patient-centricity in global research. Currently serving as the Executive Director of Project Management at Scout, Trisha oversees complex clinical trial logistics, ensuring that the operational infrastructure of research meets the highest standards of excellence. With a career…

Troy Hamilton is the Co-Founder and Director of Operations at CaRe Clinic, bringing a wealth of experience from medical research roles at the University of Calgary and senior management positions in private clinics. Renowned for his ability to transform significant initiatives into measurable outcomes, Troy leverages his background in biological sciences and project management, along…

Troy Hamilton is the Co-Founder and Director of Operations at CaRe Clinics, bringing extensive experience from medical research roles at the University of Calgary and senior management positions in private clinical settings. Renowned for his leadership excellence, Troy specializes in cultivating high-performing teams by fostering collaborative, innovative, and inclusive cultures. Through targeted leadership techniques and…

Tyron has been working in Clinical Trials for 30 years with Corporate Pharma and CROs. He specializes in Oncology trials. His passion is currently brining clinical trial opportunities to patients living in regional and remote Australia. For the past 2 years he has been the Co-chair of the Sponsors Advisory Group to the Australian Teletrial…

Van Johnson, with a decade in clinical research business development, excels in relationship-building and diversity advocacy. He serves on SCRS IncluDE and Starr Coalition’s Diversity Workgroup, is a sought-after speaker, and mentors many in the industry.

I have over 20 years experience in Clinical Trials, from both CRO and Site perspective. I specialise in startup, CTMS and finance aspects of Sponsored trials. I am a certified Change Manager, and currently studing a Diploma of Leadership. I’m an advocate of CTMS, and couldn’t do what we do without one.

Victor is an experienced executive and Global Medical Officer in Trialmed, the ThermoFisher owned clinical research site network. With 25 years experience in clinical research and drug development, he’s managed clinical trial delivery across all phases (including virus challenge) both as an academic investigator, and within the commercial setting as general manager of a global…

Having trained as a barrister & Called to the Bar by Middle Temple in 2002 my future legal career lay ahead. Unfortunately following an accident at work in 2003 I was diagnosed with a disabling pain condition; Complex Regional Pain Syndrome (CRPS). After 3 years of trying every available treatment unsuccessfully, my right leg was…

Victoria has been a part of the CNS Healthcare team since 2015 and currently serves as Vice President of Regulatory Affairs & Quality Assurance. In her leadership role, she oversees regulatory and quality operations across all five CNS Healthcare sites, promoting the highest standards of compliance, productivity, and operational integrity. With over a decade of…

Viviana is a Revenue Cycle leader with over 25 years experience in healthcare, specializing in process optimization, cross-functional team leadership, and the implementation of quality and productivity models. She currently serves as Senior Director of Front-End Revenue Cycle at Moffitt Cancer Center, leading the Clinical Trials Business Office and Financial Clearance Unit Departments. Viviana holds…

Viviënne van de Walle is a physician specialized in clinical research. She is the owner of VivHo, a life science consultancy company, and PT&R, an independent research center both in The Netherlands. She is also involved in various professional organizations in the field of clinical research, such as CISCRP, NVFG and the SCRS. For all…

Vivienne van de Walle studied medicine at the University of Maastricht in the Netherlands and did part of her medical training at the University of Oxford in the UK. During her medical training she enjoyed the combination of patient care and clinical research. She received an additional medical science degree for her research when she…

Wes Bonner brings over 25 years of experience in cultivating physician relationships and building site networks to the company. He has held key positions such as Chief Relationship Officer, Vice President/Principal Investigator Liaison, and Director of Business Development. Wes Bonner is widely recognized as a thought leader in clinical research, frequently speaking at industry conferences…

Wesley Warren is the Executive Director of Translational Research Strategy & Partnerships at City of Hope. In this role, he identifies and secures collaborations with academia, pharma, and biotech to accelerate the development of innovative cancer treatments into clinical trials. Wesley also oversees the infrastructure, expertise, and resources City of Hope utilizes to swiftly translate…

Whitney DeNeen is the Managing Director of Essential Medical Research in Tulsa, Oklahoma and Overland Park Kansas. Whitney oversees site operations, business development, and sponsor/CRO relations. With more than 15 years of experience in clinical research, Whitney is committed to ensuring her team is educated to conduct trials across a wide range of therapeutic areas…

Dr. William Smith is the CEO and one of the original founders of AMR Clinical. Dr. Smith is board certified in Internal Medicine, Critical Care Medicine, Nephrology and Cardiology and has been involved in more than 2,000 clinical trials over the past 35+ years. He is a frequent lecturer and author and publishes extensively.

Ximena Chandia is a registered nurse and midwife, she began her career in clinical pediatrics in combination with academic instruction at the University of Valparaíso. She continued in the surgery area and then embarked on clinical research as a pediatric clinical study coordinator. She has been working at Sanofi for more than 20 years in…

Xoli is responsible advancing Parexel’s drug development service offerings and ensuring delivery of innovative solutions for customers. Xoli has more than 20 years of experience in the biopharmaceutical industry in a range of roles, including clinical research, project management, and training and organizational development. Xoli earned a bachelor’s degree in medical biochemistry at Brunel University…

Yoanni Th. MATSAKIS is the Vice-President of EUCROF, the European CRO Federation since December 2024. He graduated as space and aeronautics engineer at the National High School for Aeronautics and Space (ENSAE) in France. During the period 1990 – 2000 he worked for space agencies in manned spacefilghts and conducted a R&D programme in the…

Zachariah Evangelista is a business and corporate attorney. He focuses his practice on providing legal guidance to innovative companies and entrepreneurs at all stages of growth. As a problem solver, Zachariah works with his clients to help them achieve the most efficient and effective solutions to the unique issues they face in the marketplace. Zachariah…

Global, accomplished and results oriented healthcare and life sciences business professional with experience in People Leadership, Quality & Regulatory, Complaint Management, Data Analytics, Public Speaking, and Good Manufacturing Processes . Proven track record – identify new business opportunities, build cross functional teams, and deliver impactful solutions. Regarded for the ability to identify hot spots; drive…

Zoé Felicié, is dedicated to promoting inclusivity and equity in clinical research. With over fifteen years of experience in healthcare and academia, she has developed a deep understanding of the unique challenges and opportunities in recruiting varied patient populations for clinical trials. Her work involves collaborating with research sites, service providers, and strategic partners to…