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…

Alana Cormack is an experienced Clinical Research professional with extensive local and global Project Management experience. As an Associate Director – CRA Manager she leads a team of CRAs across Australia and sits on the ANZ Leadership Team. She is a passionate advocate for Diversity, Equity and Inclusion in Clinical Trials and firmly believes we…

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 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,…

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 Acting Regulatory, Start-Up and Patient Partnership Manager at the University of the Sunshine Coast – Clinical Trials (UniSC CT), which operates six clinical trial sites across south-east Queensland. UniSC CT conducts Phase 1 to 5 clinical trials across a range of therapeutic areas in collaboration with commercial sponsors. In her role,…

I am passionate about the drug development industry and am very lucky to work in an area that continues to impact and challenge me every day. Over the past 20 years, I have worked diligently to build and refine my skills in both strategic leadership and drug development. Throughout my career, I have enjoyed various…

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…

Bio Almenia is the Senior Director of Global Feasibility and Site Engagement at Allucent, a CRO supporting small and medium-sized biotech companies with clinical research, regulatory, and biostatistical expertise. With over 25 years of experience, she has led numerous projects integrating healthcare and technology, such as EHR2EDC. Almenia’s specialties include site selection strategy, investigator identification,…

• 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…

Amir Emadzadeh is a distinguished technology leader and innovator in the life sciences and autonomous systems industries. Currently serving as Director of Software Engineering at Genentech (Roche), he leads transformative initiatives in clinical trial automation and AI-driven healthcare solutions. His groundbreaking work includes developing patent-pending platforms that have significantly accelerated clinical data workflows and enhanced…

Amitesh Sharma is a seasoned clinical operations leader with nearly two decades of experience in managing complex clinical trials across the Asia-Pacific region. As Associate Director of Clinical Operations at Telix Pharmaceuticals, a global leader in radiopharmaceuticals, Amitesh plays a pivotal role in advancing the development and execution of innovative radiopharmaceutical programs. At Telix, Amitesh…

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…

Amy Franco is the Senior Director of Patient Liaisons at Scout, where she has dedicated over 20 years to the life sciences industry. She leads with a focus on patient-centered solutions, bringing innovative strategies and strong leadership to ensure clinical trial success on a global scale. Amy joined Scout in 2002 in London, U.K., and…

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

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…

Andrew Cording is the Director of Pharmacy at St Vincent’s Hospital Melbourne, where he leads a multidisciplinary team delivering comprehensive pharmacy services across four hospital campuses. With over two decades of experience in hospital pharmacy, Andrew is renowned for his strategic leadership, commitment to medication safety, and integration of health informatics to enhance patient care….

Dr Andrew Brockway, PhD, GAICD Chief Executive Officer, Non-Executive Board Director Andrew has over twenty years pharmaceutical and research experience, including leading development and oversight of global programs, including sponsored and collaborative research trials, paediatric and adult studies, and biologicals and pharmaceutical experience. He has held strategic & leadership roles in pharma (local and global),…

Andrew commenced his career in health care over 25 years ago working as a registered nurse. During the early years working in the Cancer Services, Andrew’s interest in research was sparked that lead to a transition into this sector initially as a Clinical Trial Coordinator in 2009. Since that time, Andrew has held a number…

Ângela Papa is Executive Director and Global Study Start-Up (SSU) Lead at PPD, part of Thermo Fisher Scientific, working towards setting the global vision and strategic direction for start-up operations. With more than 20 years of experience in clinical research and operational excellence, she leads international teams to drive process integration, improve cycle times, and…

Anna Megalakakis is a Senior Training Manager at ARCS Australia with over 20 years of experience in the Contract Research Organisation (CRO) and pharmaceutical sectors. A Monash University graduate, Anna began her career in clinical research and has since held a range of roles in clinical operations and training. Her deep understanding of drug development,…

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…

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…

Antonio Hellebuyck is a Project Oversight Senior Director in the Vaccines, Government and Public Health Services at PPD, part of ThermoFisher Scientific. The PPD clinical research business of Thermo Fisher Scientific provides proven, global clinical development services to accelerate vaccine development with a dedicated vaccines delivery unit, innovative patient recruitment services, and unparalleled vaccine laboratory…

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.

Arianne brings over 20 years clinical research experience from Phase I, II, III and IV studies in both medical devices and pharmaceutical industries with responsibilities spanning all aspects of clinical research from feasibility, protocol development, study start up, monitoring, study management and medical writing. Roles have included operational and leadership positions including Clinical Affairs Manager,…

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…

Ash Clarke is the Director of Research Operations at Grampians Health and a dedicated advocate for research and clinical trials in regional and rural communities. Her experience working in research management across the research institute, academic, and public sectors for more than 15 years has provided her with firsthand insight into the complexities and challenges…

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,…

With over two decades of medical experience and a distinguished track record as an investigator in more than 40 commercially sponsored clinical trials, Barney founded Optimal Clinical Trials in 2013. He earned his medical degree from Otago Medical School in 2002 and has practiced in New Zealand, the United Kingdom, and Australia. In addition to…

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…

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 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 19 years with CNS Healthcare, I have worked as a Clinical Research Coordinator, Site Administrator, Director of Marketing, Clinical Development Liaison and Director of Contracts & Trial Management. These various roles have given me the opportunity to interact closely with patients, physicians, and study teams, and have allowed me to gain experience…

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…

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…

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…

Chantelle Courtnay is a dynamic IT leader with a proven track record in delivering secure, high-impact technology solutions across the healthcare, research, government, and entertainment sectors. At Akesa Group—a global pharmaceutical procurement and logistics company—she specialises in the management and delivery of technology initiatives that unlock operational efficiency and enhance data security, delivering value across…

Charlotte is the Associate Director of Patient Engagement at Novotech, bringing over 15 years of experience in the clinical research industry. She leads innovative recruitment strategies for global clinical trial programs, supporting a broad spectrum of therapeutic areas. With a career dedicated to enhancing patient access and engagement, Charlotte is passionate about bridging the gap…

Cheryl-Ann Hawkins is the Chief Executive Officer at Veritus Research. She has enjoyed working in many leadership positions in Clinical Trials and Oncology in a career spanning 30 years. Cheryl-Ann has in that time, had the opportunity to develop multiple clinical trial facilities and build clinical teams to ensure successful businesses. Having the right people…

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 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…

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 Packer, Victorian Comprehensive Cancer Centre Alliance – Senior Manager, SKILLED Internship & Regional Advisor Christine Packer is the Senior Manager, SKILLED internship & Regional Advisor at the Victorian Comprehensive Cancer Centre Alliance (VCCC Alliance), located in Melbourne. The VCCC Alliance is a powerful partnership between 10 leading research, academic and clinical institutions working together…

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,…

Christine has 25+ years of diverse healthcare experience spanning aged care, acute care, rehabilitation medicine, dermatology specialist clinics, and surgery. Her extensive background includes significant expertise as a clinical trial nurse coordinator and she spent 5 years in a leadership role managing the Dermatology clinical trial unit at the Skin Health Institute in Victoria. During…

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…

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…

Claire completed a MSc in Neuroscience, a PhD in Neuropharmacology and has more than 10 years of clinical and pre-clinical research experience. Claire has worked extensively in clinical trial coordination and management of Phase I-IV trials in various therapeutic areas in the UK and Australia, developing strong industry partnerships and business acumen. Claire has a…

Clara holds a Bachelor of Biotechnology and has over 10 years’ experience in the Pharma, Clinical Research Organisation (CRO) and not-for-profit sector. As the Budget and Contracts Manager at Cancer Trials Australia (CTA), Clara overseas a dedicated team of Budget and Contracts Specialists who manage CTA’s serviced clinical research sites’ clinical trial budget and contract…

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…

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 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…

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…

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 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).

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…

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…

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…

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.

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…

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,…

Emilio Neto is an executive with over 21 years of experience in Drug Development Strategy, Project Management, Clinical Operations, Team Management, and Project Finance Management globally from Phase I to Phase IV clinical trials. His expertise spans various therapeutic areas, including Rare Diseases, Respiratory, Cardiovascular, Neuroscience, Vaccines, and Oncology. Emilio began his career as a…

Experienced Chief Executive Officer with a demonstrated history of working in the pharmaceuticals industry. Skilled in Research, Management, Strategic Planning, Leadership, and Public Speaking. Strong business development professional with a Doctor of Medicine (MD) focused in Psychiatry Residency Program from Maastricht University School of Business and Economics.

Esmeralda is a Clinical Research Professional with over 6 years of experience currently serving as the Site Manager at Synexus San Antonio. She holds a bachelor’s degree in business and is an ACRP-Clinical Professional. Esmeralda has successfully led operations and strategic initiatives at her site by holding high standards for data integrity, regulatory compliance and…

Eugenia (Genie) Hong is the Clinical Trials Pharmacy Manager at The Royal Melbourne Hospital. She was a committee member of Specialty Practice in Investigational Drugs of The Society of Hospital Pharmacists of Australia (SHPA) for 15 years and has been involved in development of Standard of Practice for Pharmacy Investigational Drugs Services in Australia for…

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…

Fiona Kilkenny brings a 22-year career in healthcare to her role as Operations Manager at Emeritus research in Sydney. With a 15-year stint dedicated to clinical research, she has previous experience as a Clinical Trial Coordinator (CTC), Project Manager, and Clinical Trial Team Lead and Ethics Officer. Fiona’s involves the oversight of a diverse team…

Fransisca (Chacha) Tenorio is the Nurse Manager at NT Health Clinical Innovation and Research Unit. A registered nurse with 12 years of experience, she has a diverse background in clinical care, management, governance and research. Chacha is a passionate advocate for health equity and is committed to integrating clinical research and trials into routine healthcare…

Fre is an experienced Clinical Trial Manager with a deep passion for advancing medical knowledge through rigorous clinical research. She has successfully overseen a range of clinical trials, ensuring high-quality data collection, compliance with regulatory standards, and the safety of participants. Driven by a commitment to improving patient outcomes, she is equally dedicated to educating…

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…

With over 25 years of experience in clinical trials, Gina has held a variety of roles ranging from pre-clinical research to Senior Management. Her extensive career spans across the pharmaceutical industry, Contract Research Organizations (CROs), and site-level operations, where she brings a wealth of shared knowledge. Passionate about giving back to the industry, Gina dedicates…

Macquarie University Clinical Trials Unit (CTU) currently has nearly 200 active clinical trials across a wide range of conditions including cancer, cardiovascular, respiratory and neurological diseases. To deliver timely access for patients to novel therapies, the trials at CTU draw on: – the world-class facilities at the Macquarie University Hospital – the clinical expertise within…

Gisela Martinez is a distinguished research professional with over 20 years of expertise in clinical research. Her career is marked by a series of progressively responsible roles at the country, regional, and headquarters levels, showcasing her leadership and dedication to advancing the field. Gisela’s journey began in Australia, where she excelled in various country positions,…

Gloria has over 13 years of experience in both pharmaceutical companies as well as CROs. With a career leading innovative strategy development in a broad spectrum of therapeutic areas, Gloria is dedicated to enhancing patient centricity engagement and data driven approaches in clinical trials, especially in Asia Pac regions. With multi-lingual technical knowledge and a…

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.

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.

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…

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…

SIGAL SMS was founded by Helena Sigal, MD, who began her career in clinical research more than 20 years ago. Her various roles as medical doctor, investigator, Director of Clinical Operations, and ultimately Director of Operations at Synexus Germany provided her with extensive experience and knowledge in the field of clinical research and especially in…

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…

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 18 years in the clinical trials industry, I have enjoyed challenging and rewarding roles from Clinical Trials Research Nurse, Senior CRA, eTMF Manager to Site Care Partner. Across my career, I have worked across multiple therapeutic areas including Inflammation & Immunology, Oncology, Vaccines, and Infectious Diseases. Since joining Pfizer in 2022, I have…

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…

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…

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…

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…

Dr Jane Gaunson is the Associate Director, Local Delivery (Study Management) at GSK Australia. Holding a PhD in Immunology and Microbiology from The University of Melbourne, Jane has been a leader in Clinical Research for over 20 years where she has driven patient outcomes as a CRA, Local Study Manager, Regional Study Manager, Team Leader…

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…

Jason has over 17 years of experience in clinical research, driving operational excellence and innovation in drug development. With a strong background in clinical trial execution, he has worked across multiple phases of research, gaining insight into the evolving challenges and opportunities within the industry. In recent years, Jason has focused on advancing digital and…

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, 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…

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…

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…

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…

Jen Peterson has over 24 years’ experience in clinical research with a primary concentration in regulatory, quality compliance, and audit readiness. She has held leadership positions with 4 large CRO/AROs and currently serves as Head of Quality for M3 Wake Research, a large network of clinical research sites. She enjoys spending time with her husband…

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…

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…

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 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 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.

Josh is the Chief Technology Officer at ObjectiveHealth, an integrated research network and technology solutions company, where he leads technology strategy, engineering, and data science initiatives. With over 20 years in technology, including 15+ years in healthcare, Josh has applied his expertise in software engineering, solution architecture, systems integration, AI, and machine learning in the…

Joyce Li is a Clinical Trials Pharmacy Manager with over five years of hands-on experience at Emeritus Research. Joyce has played a key role in the initiation, coordination, and execution of clinical trials across a range of therapeutic areas. Her expertise spans investigational product management, pharmacy design, regulatory compliance, and project planning & feasibility, ensuring…

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 the Director of Business Development and Marketing at PCRN Limited and has over 18 years of experience working within the Pharmaceutical and clinical trials industry. In her current role she also is the Product Owner for the CRM system Salesforce and has a passion for technology and driving more efficient processes.

I am currently an Associate Director at Thermofisher Scientific; overseeing Project Delivery, managing diverse teams and clients. I am a motivated, highly-driven individual with a vision of bringing my best self in all that I do. I am inspired by the need to make difference, impact the world in a positive way and to elevate…

Kannan is an accomplished leader, specializing in applying technology to drive growth, quality and efficiency in small and medium sized organizations. With nearly two decades of experience across academic research institutions, technology startups, and clinical research sites, Kannan brings strategic vision and deep operational expertise to his role as CEO of Kinetic Clinical Research. Kannan…

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…

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 West is General Manager/Managing Director for Australia and New Zealand within the clinical development team at Syneos Health. Karen has over 30 years experience in the clinical trial industry of which over 22 years has been within Syneos Health through acquisition. Prior to joining Syneos Health, Karen has held a number of positions throughout…

Professor Karin Verspoor is Executive Dean of the School of Computing Technologies at RMIT University in Melbourne, Australia. Her contributions to AI and Digital Health have been recognised through selection as a Fellow of the Australian Academy of Technological Sciences and Engineering, a Fellow of the Australasian Institute of Digital Health, and as a 2021…

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…

Kate Faktor has been with Boehringer Ingelheim for since 2015 across both the Animal Health and Human Pharmaceutical areas of the organization. With a passion for collaboration, and turning consumer insights into action, Kate has more than 20 years’ experience in marketing and project management. In 2022, Kate commenced her role in patient advocacy at…

Kate has worked at Aotearoa Clinical Trials for the past six years and has a strong focus on building meaningful relationships with sponsors, investigators, and service providers to enable access to clinical research for all our communities. With a background that includes roles in both the community and private sectors, Kate brings a well-rounded perspective…

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 received her Bachelor of Science in Education from UW-Whitewater and a Master’s Degree in Exercise Physiology from UW-La Crosse. It was there, while writing her thesis, that Kathy developed her passion for research. Kathy started in the clinical research industry in 1989 working as a coordinator at the VA Hospital in Madison, WI. From…

Kathy Mickel is the Learning Solutions Lead for the Society for Clinical Research Sites (SCRS), playing a pivotal role in shaping and executing SCRS events and educational programs, including the SCRS Oncology Program. Leveraging her extensive industry experience across sites, CROs and pharmaceutical organizations, Kathy delivers engaging learning and collaboration opportunities for the clinical research…

Kathy Mickel is the Learning Solutions Lead for the Society for Clinical Research Sites (SCRS), playing a pivotal role in shaping and executing SCRS events and educational programs, including the SCRS Oncology Program. Leveraging her extensive industry experience across sites, CROs and pharmaceutical organizations, Kathy delivers engaging learning and collaboration opportunities for the clinical research…

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…

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…

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 is a highly experienced pharmacist with a diverse career spanning over two decades, both domestically and internationally. She began her career in New Zealand as a hospital pharmacy intern before expanding her expertise overseas. During her time in London, she worked with Baxter UK, specializing in aseptic sterile work, and gained invaluable experience in…

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, brings over 10 years of experience in clinical trial patient engagement, most recently serving at AbbVie. She has a proven track record of success in developing new roles and capabilities, with expertise in strategic planning, operational excellence, and business optimization. A published author and sought-after speaker, Kim has been an…

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…

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…

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…

Laura is committed to enhancing clinical trial accessibility and efficiency in ANZ. She collaborates with sites and patient advocacy groups to streamline trial operations and support the accessibility of trials within patient communities including those in regional and remote areas. Laura also organizes advisory panels to incorporate the ANZ patient voice into clinical development and…

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 Koehler, MS, CCRP, EMT-P is a seasoned leader in emergency medicine research, specializing in site operations, team development, and innovative training strategies. As a Research Manager, she oversees project managers, research coordinators, paramedics, and data support staff, ensuring efficient and high-quality research execution. With nearly a decade of experience, Lauren has pioneered creative staffing…

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….

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….

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…

Liam currently fills the role of Assistant Director of Pharmacy (Cancer Production and Clinical Trials) at the Gold Coast University Hospital, managing cancer and clinical trial pharmacy services across the Gold Coast Hospital and Health Service. Liam is a Consultant Pharmacist in Oncology/Haematology and Clinical trials and is a Fellow of the Australia New Zealand…

Lien Ho is Senior Manager of Operations for Clinical FSP at Fortrea managing a team across APAC countries working directly for a client global program. She is also the Start Up Country Manager for AUS and NZ with oversight of a team performing start up activities for studies conducted in AUS and NZ. Lien was…

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.

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…

I’m the General Manager at Optimal Clinical Trials, New Zealand’s top performing late phase clinical research group. In partnership with early phase leader, New Zealand Clinical Research (NZCR), we have seven centres across the country and able to offer you the largest, most experienced Phase 1 to 4 capability in Australasia. You can trust us…

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…

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.

Lucas commenced his role at Director – Clinical Trials at the University of the Sunshine Coast in 2015, where he oversees a team of over 160 staff working across 6 locations. Lucas has worked as an advisor, board director and consultant to various organisations specialising in clinical trial strategy development. Lucas is an Executive Committee…

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…

Luis has over 25 years of experience in clinical trials. He is a world trotter professional who has lived and worked in Europe, US and Asia. He has a wide range of expertise that includes, just to name few, clinical operations, feasibility strategy, site relationship development and management, and decentralized engagement solutions. Luis is an…

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…

I am a Clinical Research Professional with over a decade of experience in the CRO industry, I have gained comprehensive insights working in both full-service and outsourcing models. My career has spanned various roles, from entry-level positions to management, providing me with a holistic understanding of the clinical research landscape. My expertise includes managing Phase…

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 Sr. Director of Security, Corporate QA and Compliance, 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…

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…

As a Consultant Pharmacist in Clinical Trials and Oncology/Haematology, Liam fulfils the role of the National Research Lead and Cancer Care Educator – Pharmacy for Ramsay Health Care. In this role he is responsible for strategy delivery and workforce development nationally in these specialist areas. Liam is a member of the SHPA Clinical Trials Leadership…

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 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 has worked in the clinical research industry since 2000, with a background in sales, sales management and commercial leadership across Asia Pacific, Europe and the US for Contract Research Organisations in the main. In 2015 he sought and attained capital funding for a new company, Paratus Clinical of which he is now a Director,…

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…

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 has 17 years of clinical trials experience working in a range of roles within IQVIA and within the Australian + New Zealand clinical research industry. She is committed to the implementation of flexible, patient-centric, site-friendly and solution focused delivery methods in all aspects of clinical trials, resulting in positive outcomes for patients. Megan’s current…

Melanie’s career spans more than 20 years across the therapeutic development lifecycle and digital technology. She is currently the Director of User Experience Research & Strategy in the Digital Products and Solutions (DPS) organization at IQVIA. She brings a human-centered lens to complex healthcare and technology challenges, helping to uncover user needs and strategic opportunities,…

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 Simpson leads the Oceania Clinical Development Centre at Novo Nordisk, overseeing clinical trial strategy and execution across Australia and New Zealand. With close to 20 years in the research, pharmaceutical and CRO sectors; she brings deep expertise in trial design execu-tion, regulatory strategy, and cross-functional leadership. Melissa has experience executing clinical trials with a…

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…

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 Rogan is the Senior Director, Mobile Application Experience at Greenphire, where he is responsible for developing products to support participant success in clinical trials. Michael started his work life building financial software on Wall Street, and then got a PhD in Behavioral Neuroscience, publishing research on how information is processed in dangerous/stressful conditions. Michael…

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…

Michele Leggott’s latest book of poetry, Face to the Sky, explores her encounter with 19th-century New Zealand botanical artist Emily Cumming Harris. But there’s more to this story – Michele was battling non-Hodgkin’s lymphoma while working on the book. In early 2020, Michele received her diagnosis, just as the Covid-19 lockdowns began. Chemotherapy, radiotherapy, and…

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 Gallaher is a Melbourne-based award-winning entrepreneur, speaker and advocate for the Australian health technology sector and for women in science, technology, engineering maths and medicine (STEMM). As CEO of Opyl Ltd (ASX:OPL) a company working at the intersection of social media, clinical trials, health data and artificial intelligence, Michelle is a sought-after mentor, collaborator,…

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…

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…

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…

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…

Murtaza brings over 13 years of extensive experience in the fields of business analytics, management, and multifaceted roles in marketing, technology, and business growth. With a proven track record of driving strategic initiatives and delivering tangible results, he has become a seasoned professional in navigating the dynamic landscape of modern business. A key driver of…

Nach is a seasoned professional with over 17 years of experience in clinical development, specializing in business expansion and strategic growth. He has held key positions across industry-leading organizations, from strategic consulting firms to top CROs, where he has played a pivotal role in driving revenue and fostering partnerships. In his recent roles at Parexel,…

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).

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…

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…

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…

Nicola Chapman heads up the thriving Macquarie University Clinical Trial Unit. She has helped grow the unit from a team of 19 staff just 6 years ago to more than 100 staff now. The CTU manage more than 600 active patients across more than 200 trials at any one time. The centralised CTU supports any…

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…

Noelle Saldana is the Head of Research Analytics (AI & ML) for the Rapid Development Studio for AI/ML at Fortrea, where she drives innovative solutions that accelerate clinical trials and research innovation. With over 15 years of experience at the intersection of data science, AI, and strategic leadership, Noelle has driven transformative initiatives across startups,…

Oscar Tunjic is the Operations Manager at Emeritus Research’s Melbourne facility. Since joining the organization in 2019, Oscar has steadily grown into leadership roles, including several years as a Study Coordinator. He has worked extensively on vaccine trials, particularly those requiring high recruitment volumes in short timeframes. With a Graduate Diploma in Clinical Research, Oscar…

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, an Australian health tech company transforming how clinical trials are recruited, tracked, and delivered through technology-led operations and participant-first engagement. Pam brings a unique blend of strategic, commercial, and technical expertise to the table. She began her career at Luminary, now one of Australia’s most prominent digital agencies….

Paul Christensen is the Co-Founder of Life Clinical Research and a recognised leader in clinical trial operations across Australia and New Zealand. A Registered Nurse and graduate of Queensland University of Technology, Paul has worked in clinical research since 2004, beginning as a Study Coordinator and progressing to roles in site network management, project management,…

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 Lee is a registered hospital pharmacist with over 20 years of experience, specializing in clinical trials and investigational drug services. She holds a Bachelor of Pharmacy from Monash University and a Graduate Diploma in Clinical Research from the University of Melbourne. Paula was an expert reviewer for the Human Research Ethics Committee (HREC) at…

Penny is a co-founder of Optimal Clinical Trials, part of the NZCR Group, a clinical trials group with sites throughout New Zealand. Optimal specialises in late phase (Ib-III) clinical trials in a wide range of therapeutic areas, and together with NZCR who are early phase experts, the NZCR Group provide sponsors and CROs expertise in…

Peter Koefler serves as the Process Excellence and Delivery Director at Takeda Pharmaceuticals. In this role, he is dedicated to helping to further the strategic advancement of Clinical Site Startup & Engagement (CSSE) through innovation and excellence. Peter leads and supports the implementation of process optimization by aligning with business practices. He possesses extensive experience…

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,…

Pip has over 25 years’ experience in clinical research and over 15 years’ experience managing high performing teams. Pip has a unique understanding of all the stakeholders involved in delivery of clinical trials, having held senior roles in CROs, pharmaceutical companies and at sites. Pip has a passion for simplifying operations and increasing efficiency, so…

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…

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.

Ramy Nassar is the AI Innovation Lead at Signant Health, where he drives the development and adoption of cutting-edge AI solutions to transform clinical trials and digital health. A futurist, author, and technology strategist, Ramy helps organizations anticipate what’s next and harness emerging technologies to unlock new value. He is an internationally recognized keynote speaker…

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 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…

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…

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…

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…

Rima Darwiche, the 2023 Women In Leadership Awardee from BioMelbourne Network, is a highly accomplished professional with a passion for improving patient access to life-saving therapies. Holding a Bachelor of Medical Science in Immunology from the University of Melbourne and a PhD scholarship, Rima transitioned to a career in pharmacy to connect with patients directly….

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…

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…

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 proficient clinical research professional with over 20 years of experience in clinical trials, including extensive expertise across all phases of research, from first-in-human (Phase I) to large-scale Phase IV studies, with knowledge of the New Zealand clinical research environment and experience spanning Asia-Pacific and Europe. Throughout her career, Ruth has always…

Sally is a skilled leader, project and partnerships director with over 25 years of experience working across Australian and global government, industry and academic organisations. Her experience spans diverse sectors including education, training, biotech, science, health and the pharmaceutical sectors. Recent roles have included leading the Victorian public-private partnership office for the world’s largest healthcare…

Clinical Trials Pharmacy Manager with nearly 20 years of experience in the healthcare industry, spanning retail pharmacy, hospital pharmacy, and clinical trials. Over the past six years, my primary focus has been on delivering pharmacy services for Phase 1 First-in-Human (FIH) clinical trials, ensuring the safe, efficient, and compliant management of investigational products. My expertise…

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….

Samir Jain is a Senior Director of Product Management, responsible for building Medidata’s EHR Integration strategy and Site solutions. Samir has over 20 years of experience working with healthcare technologies and organizations. Samir started his career building EHRs, leading the interoperability and standards team at Allscripts. He later spent time building large scale Health Information…

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…

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…

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 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 Schliebner is a strategic and innovative drug development executive with 30 years of experience across the biopharma, contract research organization (CRO), and non-profit sectors. Passionate about ensuring the patient voice is incorporated into drug development, Scott emphasizes patient-focused solutions to reduce the burden of clinical trial participation and accelerate drug development. Scott serves as…

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…

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…

Extensive clinical experience and over 24 years research experience across both investigator-initiated studies and pharmaceutical sponsored clinical trials. She is a Registered Nurse, Transcelerate accredited ICHGCP trainer and current PhD Candidate at the University of Sydney studying Enablers and Barriers to conducting Research within the Public Health System in NSW.

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…

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…

Passionate about new drug development and commercialization with a demonstrated history of delivery in R&D and the clinical trials industry. Skilled in Change and Risk Management, Negotiation, Fast-Moving Consumer Goods (FMCG), Operations Planning and Management, Coaching, and Strategic Planning. Strong program and project management professional with a Master of Science.

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…

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…

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 Marshall, General Manager – New Zealand for Momentum Clinical Research, provides leadership for the eight MCR sites across New Zealand, bringing a wealth of experience and expertise in executive and health management. Sue’s leadership is people-centered, with a strong focus on fostering collaborative teamwork and individual growth. Before joining Momentum, Sue served as CEO…

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 Night is responsible for creating TD2’s strategic vision and working across the company to execute the subsequent initiatives that sustain and grow the organization. Susan has 25 years in the healthcare and clinical research industries spanning strategic planning, regulation, policy, and law. Susan served as a Senior Health Policy and Ethics Fellow for the…

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…

Associate Director with over 25 years of clinical research experience in pharmaceutical and CRO companies. Renowned for strong leadership and people management skills within matrix-driven global organizations. Proven track record in nurturing early talent and fostering cross-collaboration with stakeholders. Multi-lingual with robust technical knowledge in operations and a deep understanding of the Asia Pacific region.

Suzanne is the Greenslopes Private Hospital’s Gallipoli Medical Research’s (GPH-GMR)-Associate Director of Clinical Trials. In a prior role, she was Operations Manager, Scientific Officer and Deputy CEO of Q-Pharm for over 13 years, a Brisbane-based, Early-Phase clinical trial site company. Starting as a Medical Laboratory Scientist working at many of the east-coast private pathology providers,…

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…

Swetha Khokale is an accomplished professional with over 19+ years of experience across various facets of clinical research. Currently serving as Country Head, India at Advarra, she oversees business operations, global support services and the India product and technology teams of 450+ professionals that work with global sites, sponsors, CROs and research stakeholders to decrease…

Senior leader with 15+ years in Asia Pacific developing strategy and driving operational delivery to by bring potentially life-saving or life changing medication to market faster. Experienced in building, managing, and growing operational teams across both the APAC region and globally. Skilled in developing, planning, and implementing transformational delivery models and successful integrations. I am…

My expertise is in clinical trials operations, education/ workforce development. Overall, I have over 16 years clinical trials experience and for the past 7 years my focus has been on developing clinical trials education models for effective workforce upskilling. My current role within TrialHub extends to working with the diverse health services within our partnership,…

Tina has 20 years’ experience working in the public health sector in both Australia and the UK and has over 15 years’ experience working in clinical trials. As the Data Manager/Study Coordinator at Department of Molecular Imaging and Therapy at Austin Health, Tina overseas a number of trials from Phase 1 to 3 in both…

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,…

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…

Tori Furner is a Clinical Trial Operations Manager and strategic project leader with expertise in early-phase research, including first-in-human (FIH), vaccine, heamatology, oncology, healthy volunteer, and other patient studies. She currently leads the South Bank clinical trial site team within the University of the Sunshine Coast’s network, overseeing a portfolio of trials and directing a…

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…

Tyler Mathes is a seasoned marketing professional with over two decades of experience. His early career saw him as a marketing leader for revered global brands, including Bang & Olufsen, Georg Jensen, and Neuw Denim, where he honed his expertise in brand development and market engagement. In 2017, Mathes leveraged his extensive background to found…

Tyron has thirty-three years in pharmaceutical industry conducting clinical research as a CRA, project manager, research manager and currently a clinical development consultant with Eli Lilly Australia. Tyron is currently the Co-chair of the Sponsors Advisory Group for the Australian Teletrial Program.

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.

23 years Clinical Trial Experience both CRO and Site. Specialising in Startup Activity (Budgets & CTMS). Currently (8 years) at a VERY paper based Site, introducing technology to streamline processes.

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…

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…

Vivian Huey is a Site Alliance Manager at Genentech, where she leads efforts within the Advancing Inclusive Research (AIR) Site Alliance, a national consortium of sites focused on improving representation and equity in clinical trials. In this role, she manages site partnerships across the U.S., helping ensure sites are positioned for success through best practice…

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…

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…

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…

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…

Wayne is Senior Vice President, Data Experience (including Rave EDC, Medidata Clinical Data Studio, Medidata Designer, Rave Imaging, Rave RTSM, Rave Coder, and Rave Safety Gateway) at Medidata. His responsibilities include the strategy, development, and delivery of these products across all Research & Development disciplines. Before joining Medidata, Wayne spent 12 years overseeing Product Management…

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…

Over the 25 years, Bill has taken up roles of increasing responsibility in Medical Affairs and Clinical Development. Bill moved to Pfizer HQ, New York in 2004 as Regional Medical Director of Japan/Asia in cardiovascular medicine. In 2009, he became the Clinical Development Lead of Emerging Markets for medicines in the treatment of heart &…

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.

Yvonne began her career in academic “bench” research with Adelaide University and CSIRO. Yvonne then moved into clinical trials research at a dedicated Phase I unit where she was one of the first in Australia to test a new chemical entity in healthy volunteers, giving rise to what is now a strong Phase 1 sector…

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…