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Job description
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 attributes
uro-oncology focus, regulatory review, Medical Affairs leadership, cross-functional collaboration, patient-centric communication, hybrid work model with travel up to 60%.
Location and Work arrangement
Princeton, NJ (Hybrid).
No specific trial phases or modalities beyond oncology and urologic cancers are mentioned.
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Worksite address
princeton, NJ, 08543, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.