I bring over 20 years of Clinical Research Experience within the Medical Device and Pharmaceutical industries, where my responsibilities have included designing, implementing and managing clinical studies that align with strategic goals and comply with regulations at both a local and international level.
I have worked across all phases of clinical research and managed and developed clinical studies across both pharmaceutical and medical device disciplines. This has included collaboration with corporate head offices and working closely with KOLs to develop protocols within their interest areas.
I am a structured, dedicated, motivated individual with a passion for clinical research. My focus on quality and meticulous attention to detail have allowed me to develop into a role of SOP creation and implementation of Clinical Research Quality systems, which have created a high quality approach to clinical trials that are fully aligned with regulatory, ethical and legal requirements within the global research environment.
Specialties: Medical Devices, Pharmacology, Oncology (Breast, Lung, Colorectal, paediatric), Cardiac Rhythm Disease Management, Respiratory, Metabolic disorders, Immunology, Quality Systems, Training, SOP development and oversight, Protocol development, Ethics Submissions, Project Management.