Associate Director, Medical Affairs

Role: Associate Director, Medical Affairs responsible for leading Medical Communications and Medical Information functions within a biopharma specializing in uro-oncology. Objectives include ensuring compliant scientific communication, review of promotional and nonpromotional materials, and efficient Medical Information operations. Responsibilities: lead PARC/MRC review processes, coordinate cross-functional reviews, ensure accuracy and compliance of materials, and maintain documentation; support Medical Information inquiries, develop resources, and train staff. Requirements: PhD, PharmD, or similar doctorate; extensive experience in medical, legal, and regulatory review within biotech/pharma; strong scientific background in oncology or rare diseases preferred; excellent communication, leadership, and stakeholder management skills. High-value: uro-oncology focus, regulatory review, Medical Affairs leadership, cross-functional collaboration, patient-centric communication, hybrid work model with travel up to 60%. Location: Princeton, NJ (Hybrid). No specific trial phases or modalities beyond oncology and urologic cancers are mentioned.