Associate Director of Scientific Affairs, Site Activation Liaison
For over 15 years, Ms. Coburn has been an active participant within the clinical research industry. She has experience in document management, overseeing FTLs and key sponsor portfolios, in Early Development Services as a medical writer specializing in protocols and CSRs for Phase I projects, and most recently within Global Study Start-Up. Ms Coburn was a key contributor in the development of a Site Partnerships group at ICON, managing the CROs relationship with our key site network contributors, and creating processes and relationships to ensure KPIs were met across the company. Additionally, she has trained multiple teams globally, on both Start-Up and Site Partnership processes. Ms Coburn is passionate about site relationships and her experiences provide her with a unique perspective on an industry that is so valuable in bringing life-changing treatments to patients in need.