TAS - Key Persons
Sarah Day is an independent consultant and freelance senior clinical research associate with over 13 years of experience in clinical trial research. Her experience covers an expansive range therapeutic areas, including: oncology, haematology, pharmacokinetics, bioequivalence, cardiovascular, critical and intensive care, endocrinology, osteoarthritis, neurology, OTC therapeutics, smoking cessation and social/behavioural, and musculoskeletal trials. She has worked in both Australia and the United States, giving her a thorough understanding of both TGA and FDA regulations and guidelines, including ICH-GCP. She has extensive experience with in-house monitoring, project management, study start-up, product and device registration, auditing of trials, working for pharmaceutical companies, clinical research organisations, GCP compliance audits and as an independent consultant.
Areas of Expertise
Over 12 years of experience has afforded the opportunity to develop a wide range of skills in the field of clinical research, including, but not limited to:
Sarah Day has an excellent reputation with her previous employers, which include internationally renown pharmaceutical companies, CROs and medical centres. References are available upon request.