Medical Director (Oncology)
Genmab
October 1, 2026
Full-time
Remote friendly (Princeton, NJ)
Worldwide
Clinical Research and Development
Role: Medical Director (Oncology) at Genmab, responsible for medical oversight of clinical trials, data review, and contribution to regulatory documents within cancer therapeutics. Responsibilities include designing and executing pivotal cancer studies, shaping medical strategy, generating/reg reviewing clinical documents (regulatory submissions, dossiers), ensuring document quality, and leading external/internal stakeholder interactions (regulatory authorities, KOLs, advisory boards). The role also oversees patient safety, plans publication strategies, and supports team development and mentoring. Requirements: MD with at least 3 years' industry experience in oncology or hematology, experience as a Medical Officer in clinical trials, and a strong understanding of solid tumor oncology. Proven ability to represent the company externally and collaborate cross-functionally. Preferred: deep scientific background in oncology and prior experience with regulatory or late-stage clinical development. HighValue: oncology, solid tumors, clinical trials, medical strategy, regulatory documentation, stakeholder engagement, mentoring. WorkSetup: flexible remote work (20-40%), with some travel likely.