Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Pfizer

Clinical Development Medical Director – Associate Director

Pfizer

. Provides medical monitoring on one or more clinical trials .

Posted 5/6/2026full-timeCollegeville • California, Illinois, New York, Pennsylvania • 🇺🇸 United StatesSenior💰 $189,200 - $315,400 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
  • Contributes to medical assessments of Quality Events
  • Conducts and documents periodic safety data review and ongoing clinical/medical data review
  • Reviews Required Safety Text for the Informed Consent Document
  • Provides clinical support for one or more studies
  • May provide input to the protocol design document
  • Supports the study team in internal protocol review governance submissions and interactions
  • May develop Study Informed Consent Documents
  • Provides clinical input to the development of the Statistical Analysis Plan
  • Ensures all clinical queries are appropriately addressed in support of database lock
  • Tracks and reconciles Serious Adverse Events
  • Contributes to site selection criteria
  • May serve as a clinical point of contact with investigators and study team for questions relating to clinical aspects of the protocol

Requirements

What you’ll need
  • Obtained a primary medical degree (e.g., MD, DO, MBBS, MBChB) from a recognized medical school/university
  • 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
  • Maintained registration/Medical License to practice and always in good standing with their Medical Licensing Authority
  • Clinical research experience in the biopharmaceutical industry in study design, start-up, conduct, and close-out, including regulatory submissions and inspections
  • Scientific productivity via publications, posters, abstracts and/or presentations
  • Knowledge of clinical development, global and regional regulation, and ICH/GCP
  • Clinical and administrative capabilities; effective verbal and written communication skills
  • Track record of achievement in pharmaceutical development

Benefits

Comp & perks
  • 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 including medical, prescription drug, dental and vision coverage

ATS Keywords

✓ Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical monitoringmedical assessmentssafety data reviewclinical data reviewprotocol designStatistical Analysis Plandatabase lockSerious Adverse Events trackingsite selection criteriaclinical research
Soft Skills
effective communicationclinical supportteam collaborationproblem-solvinginterpersonal skillsorganizational skillsleadershipattention to detailcritical thinkingadaptability
Certifications
MDDOMBBSMBChBMedical License