Sara Croteau

Associate Director, Clinical Operations - Quality Management

Innovaderm

Sara Croteau has extensive experience in clinical trials ranging from phase I to III (including pk studies, bioequivalence studies). Sara started her career managing trials at a Clinical Research site with in-patient capability's, as a Site Manager. Sara then worked in the Pharmaceutical, Biotech and CRO environments, managing the full scope of activities such as Investigator and site selection activities, training and mentoring staff, identifying and resolving study site issues, assisting in writing and updating SOPs, overseeing incumbent CROs and vendors, serving as a primary contact with sponsors and ensuring that deliverables are provided on time and within budget. Most recently, she has been involved in the update of risk management SOPs and associated training of clinical trial staff.

Session

• The ABCs of Risk-Based Monitoring for Sites