Director, Global Medical Evidence Generation Lead, Oncology

Role: Director of Medical Evidence Generation in Medical Affairs, focusing on strategic planning and execution of evidence studies for Oncology assets, including clinical trials, RWE, and observational research. Responsibilities: define integrated evidence strategies aligned with medical and product goals; develop study protocols ensuring scientific and operational rigor; lead or contribute to study design, governance, and scientific dissemination; partner across functions (Medical Strategy, Clinical Development, HEOR, RWE, Regulatory) and external investigators; ensure compliance with GCP and ICH guidelines; manage CRO/vendor relationships; participate in scientific forums and publications. Requirements: advanced degree (MD, PhD, PharmD, MS), 5+ years in pharma clinical development or Medical Affairs, deep oncology expertise, strong strategic and scientific acumen, proven ability to lead cross-functional teams, and global stakeholder engagement. Preferred: experience with Phase II/IV research, real-world evidence, and investigator-sponsored studies. High-Value: oncology, evidence generation, clinical trial design, RWE, cross-functional collaboration, global travel (~20%), based in Lawrenceville or Madison, NJ.