Define the clinical operations strategy and ensure execution of clinical trials end-to-end
Manage day-to-day operations of assigned studies
Lead cross-functional teams and ensure vendor compliance
Establish clinical trial budgets and track financial status
Perform ongoing vendor management and oversight
Ensure inspection readiness at all times
Monitor and communicate with CROs to ensure data currency

Advanced degree (MS/PhD, PharmD) in life sciences preferred with a minimum of 6 years clinical trial management experience
Strong knowledge of ICH/GCP/FDA regulations, site monitoring/CRA experience is required
Proven clinical study management skills
Experience with complex/rigorous study designs
Well-developed written and verbal communication skills
Analytical and problem-solving capabilities
Ability to travel to domestic and/or international sites as needed
Ability to travel to New York City HQ as needed

Associate Director, Clinical Trial Management

Key skills