Clinical Development Medical Director (MD required)
Pfizer · Pearl River, NY +2 more
Medical AffairsFull-time$240k–$400kCompany career page
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Role summary
Pfizer seeks a Medical Director to oversee clinical trial design, execution, and safety monitoring across multiple studies. The role involves medical strategy development, regulatory engagement, and cross-functional collaboration to ensure patient safety and data quality throughout the clinical development lifecycle.
What they're looking for
- Medical degree (M.D., D.O., or equivalent)
- 4+ years of work experience in pharmaceutical industry
- Licensed to prescribe medicines independently for minimum 2 years post-internship
- Documented clinical research and registration activity experience
- Ability to critically evaluate medical and scientific information
- Understanding of clinical program design, development, and execution
What you'll be doing
- Oversee study safety through regular review of individual and cumulative safety data with risk leads
- Design clinical protocols and development strategies aligned with regulatory requirements and program objectives
- Conduct medical review and interpretation of efficacy and safety trial data with statisticians and writers
- Provide medical guidance to study teams, investigators, and site personnel on protocol compliance and patient safety
- Author clinical sections of regulatory documents including Investigator Brochure and clinical study reports
Privacy & handoff
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