Associate Director, Clinical Sciences, Oncology

Role: Support clinical development of Moderna's Oncology programs, focusing on Phase 1-3 trials to ensure data quality for regulatory and internal decisions. Responsibilities: collaborate with Clinical Study Lead and teams to oversee trial design, start-up, safety monitoring, data review, and closeout; contribute to regulatory documents; assist in site management and inspection readiness; support investigator engagement activities; and promote process improvements. Requirements: PhD, PharmD, Masters, or advanced nursing degree with significant oncology knowledge; 8+ years in pharmaceutical/biotech clinical development; experience with clinical data analysis, Medidata Rave, and data platforms preferred; strong communication skills; willing to travel up to 15%. HighValue: oncology (specific therapeutic focus), Phase 1-3, data integrity, regulatory document authorship, clinical trial oversight. WorkSetup: based in Cambridge, MA or Princeton, NJ, with 70% onsite and up to 30% remote.