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Pfizer

Clinical Development Medical Director, MD Required

Pfizer

. Provides medical monitoring on one or more clinical trials .

Posted 5/7/2026full-timeCollegeville • California, Connecticut, Illinois, Massachusetts, Pennsylvania • 🇺🇸 United StatesLead💰 $239,900 - $399,800 per yearWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Provides medical monitoring on one or more clinical trials
  • Provides timely, study-related medical information and guidance
  • Conducts and documents periodic safety data review and ongoing clinical/medical data review
  • Reviews required safety text for the Informed Consent Document
  • May independently lead clinical execution of one or more studies
  • Represents the study team in internal protocol review governance submissions
  • Ensures development of Study Informed Consent Documents
  • Develops site selection criteria and provides clinical input to selection of sites

Requirements

What you’ll need
  • Obtained a primary medical degree (e.g., MD, DO, MBBS, MBChB) from a recognized medical school/university
  • 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
  • Cardiometabolic disease experience, e.g., obesity, diabetes, endocrinology, etc.
  • Scientific productivity via publications, posters, abstracts and/or presentations
  • Extensive knowledge of clinical development, global and regional regulation, and ICH/GCP

Benefits

Comp & perks
  • Health benefits including medical, prescription drug, dental and vision coverage
  • 401(k) plan with Pfizer Matching Contributions
  • Pfizer Retirement Savings Contribution
  • Paid vacation
  • Paid holiday and personal days
  • Paid caregiver/parental and medical leave

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
clinical trialsmedical monitoringsafety data reviewclinical data reviewInformed Consent Documentsite selection criteriaclinical researchbiopharmaceutical developmentscientific productivityICH/GCP
Soft Skills
leadershipcommunicationorganizational skillsteam representation
Certifications
MDDOMBBSMBChBlicensed to prescribe medicines