Director, MEG Lead Cardiovascular, Medical Evidence Generation

Role: Director of Medical Evidence Generation in Medical Affairs, focusing on the Cardiovascular (CV) portfolio. Responsibilities include developing and executing comprehensive evidence strategies through clinical trials (Phase II/IV), real-world evidence, and observational studies to support product development, value demonstration, and medical strategy. The role involves scientific leadership in study design, protocol development, partnership with CROs, and engagement with KOLs and external research partners. It requires ensuring regulatory compliance (GCP, ICH), managing study lifecycle, and scientific dissemination. Qualifications: Advanced degree (MD, PhD, PharmD, MS) with 5+ years in pharmaceutical clinical development or Medical Affairs, with CVRM experience. High-value specifics include a focus on CV therapeutic area, clinical trial oversight, real-world evidence, and cross-functional collaboration across Medical Strategy, HEOR, Regulatory, Clinical Operations, and external stakeholders. Travel is expected at 20-30%. Work location options are Lawrenceville or Madison, NJ.