Associate Director, Medical Affairs

Scorpion Therapeutics; Princeton (NJ); Hybrid; USD 180,000 - 240,000; Full time

Benefits offered by this job

Hybrid work model

Travel up to 60%

Job summary

Scorpion Therapeutics seeks an Associate Director of Medical Affairs to lead Medical Communications and Medical Information within a biopharma focused on uro-oncology. The role emphasizes compliant scientific communication, review of materials, and efficient Medical Information operations.

The position requires a doctorate and extensive regulatory review experience, with hybrid work in Princeton, NJ and travel up to 60%.

Qualifications

• Experience leading medical communications review processes.
• Strong stakeholder management and leadership abilities.
• Proven ability to train staff and develop resources.

Responsibilities

• Lead PARC/MRC review processes and coordinate cross-functional reviews.
• Ensure accuracy and compliance of materials and maintain documentation.
• Support Medical Information inquiries and develop patient-focused resources.

Skills

Medical Affairs leadership

Regulatory review

Cross-functional collaboration

Oncology expertise

Uro-oncology focus

Education

PhD/PharmD or equivalent

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.