Senior Medical Director, Clinical Development & Strategy

Pfizer Inc; Collegeville (PA); Hybrid; USD 189,000 - 315,000; Full time

Benefits offered by this job

401(k) with Pfizer matching

Retirement Savings Contribution

Paid vacation, holidays and personal/2

Comprehensive health benefits (medical

Parental/Caregiver leave

Job summary

Pfizer Inc. seeks an Associate Director, Clinical Development Medical Director to ensure the medical and scientific integrity of studies and the wellbeing of patients enrolled in multiple trials. The role applies advanced clinical and design principles to deliver high-quality trials and operational excellence.

Hybrid work arrangement in the United States with global development leadership support. Requires an MD/DO and phase 3/pivotal experience, strong writing skills, and the ability to

Qualifications

• Medical degree and clinical research experience.
• Licensed to prescribe medicines for at least 2 years post intern.
• Clinical research experience in phase 3/pivotal space.
• Strong scientific writing with publications, posters, abstracts, or presentations.

Responsibilities

• Perform medical monitoring on one or more clinical trials and address medical questions from investigators and site personnel.
• Lead safety data reviews and ongoing clinical/medical data reviews.
• Contribute to protocol design and development; ensure efficient protocols and site engagement.
• Provide clinical/medical input to data collection tools and SAP/TLFs/BDR.
• Establish Data Monitoring Committees and endpoint adjudication processes; manage risk review plans.
• Interface with external investigators and internal study teams on protocol-related clinical/medical questions.

Skills

Clinical Research

Medical Monitoring

Regulatory Knowledge

Risk Management

English Communication

Education

MD/DO/MBBS/MBChB

Medical License

Tools

AI Tools

Job description

Pfizer Inc. seeks an Associate Director, Clinical Development Medical Director to ensure the medical and scientific integrity of studies and the wellbeing of patients enrolled in multiple trials. The role applies advanced clinical and design principles to deliver high-quality trials and operational excellence.

Hybrid work arrangement in the United States with global development leadership support. Requires an MD/DO and phase 3/pivotal experience, strong writing skills, and the ability to