Clinical Development Medical Director

Role Overview

The Clinical Development Medical Director is responsible for medical and scientific oversight, data integrity, and quality of clinical trials in Internal Medicine. They will provide medical monitoring on one or more clinical trials, contribute to medical assessments of Quality Events, and conduct periodic safety data review and ongoing clinical/medical data review.

What You Will Do

The successful candidate will provide timely, study-related medical information and guidance, review Required Safety Text for the Informed Consent Document, and lead clinical execution of one or more studies. They will also represent the study team in internal protocol review governance submissions and interactions.

Why It Might Be a Fit

The ideal candidate will have 4+ years of experience in biopharmaceutical industry in clinical research and development, a primary medical degree (e.g., MD, DO, MBBS, MBChB), and be licensed by a licensing body/health authority to prescribe medicines independent of Supervision for at least 2 years post their intern/house officer/foundation period.

Requirements

• Primary medical degree (e.g., MD, DO, MBBS, MBChB)
• 4+ years of experience in biopharmaceutical industry in clinical research and development
• Licensed by a licensing body/health authority to prescribe medicines independent of Supervision for at least 2 years post their intern/house officer/foundation period

Benefits

• 401(k) plan with Pfizer Matching Contributions
• Pfizer Retirement Savings Contribution
• Paid vacation
• Holiday and personal days
• Paid caregiver/parental and medical leave
• Health benefits to include medical, prescription drug, dental and vision coverage