Medical Director/Senior Medical Director, Clinical Development

Responsibilities

• Serve as the primary Medical Monitor for global clinical studies
• Provide ongoing medical review of safety, efficacy, and eligibility data
• Evaluate and assess serious adverse events (SAEs) and emerging safety signals
• Collaborate with Pharmacovigilance for signal detection and risk management
• Provide medical oversight of study execution from initiation through database lock
• Support protocol development, amendments, and informed consent forms
• Act as a primary medical contact for investigators and study sites
• Conduct ongoing review of accumulating safety and efficacy data
• Support preparation of regulatory submissions and health authority interactions
• Present clinical updates to internal governance committees and senior leadership

Requirements

• MD, DO, or equivalent medical degree
• Minimum of 3+ years industry clinical development experience
• Board certification or training in Oncology, Hematology/Oncology, Internal Medicine, or a related specialty
• Experience serving as a Medical Monitor for interventional clinical trials
• Working knowledge of GCP, ICH guidelines, and global regulatory requirements
• Strong understanding of oncology drug development and clinical trial conduct

Preferred Qualifications

• Experience supporting Phase 2 and/or Phase 3 oncology studies
• Experience with rare diseases, sarcomas, or desmoid tumors
• Experience supporting regulatory submissions and health authority interactions
• Experience working within a matrixed, cross-functional environment

About the Company

Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies, including antibody-drug conjugates.