Clinical Development Medical Director, GU

Pfizer seeks a Clinical Development Medical Director to provide medical and scientific leadership for a Phase 3 prostate cancer oncology trial. The role encompasses study oversight, medical monitoring, safety evaluation, data interpretation, and regulatory document development across a global matrix organization.

Responsibilities

• Serve as Medical Monitor and provide clinical leadership for Phase 3 prostate cancer trial
• Conduct medical monitoring including eligibility consultation, adverse event review, and safety surveillance
• Lead development and review of clinical protocols, informed consent documents, and regulatory submissions
• Collaborate with cross-functional teams on data review, interpretation, and analysis plans
• Engage with investigators, health authorities, and governance bodies on study strategy and risk mitigation

Requirements

• Medical degree (MD or DO) with oncology clinical expertise
• Experience as medical monitor or clinical development medical director
• Strong knowledge of prostate cancer treatment and clinical practice
• Demonstrated ability to lead across matrix organizations and external stakeholders
• Proficiency in regulatory affairs and health authority interactions
• Excellent medical writing and scientific communication skills