Lee A.

Background

About Lee A.

Since joining the clinical research industry in 1998, I've held various clinical and management positions with niche, mid-sized and major CROs, as well as small pharma. Through these experiences I've gained invaluable knowledge and insights from the Sponsor, service-provider and Investigator Site perspectives. • 20+ years of combined CRO and Pharma multi-disciplinary clinical experience with increasingly expanded roles and responsibilities • 10+ years in Sr. PM, PM, Clinical Study Manager, and Clinical Project Manager capacities • Management of clinical and full study budgets up to $17M • NDA preparation, review and submission experience • 6+ years in CRA / Monitoring roles with various EDC platforms • Oncology expertise with early phase development focus • Other therapeutic experience includes: Neurology, Movement Disorders, Infectious Disease, and metabolic disorders • Managerial experience under direct and matrix models, including both local and remote staff • Dedicated to relationship-focused, cooperative interactions with Sponsors, Investigators/Site Staff and internal teams. My aim as a Project Management / Clinical Operations professional is to support and advance the science, the processes, and the relationships that will ultimately lead to the availability of expanded treatment options for patients and their health-care providers.