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Associate Director, Clinical Pharmacology
PfizerLeading clinical pharmacology studies and providing expertise in oncology development programs at Pfizer. Collaborating with multidisciplinary teams to optimize drug development processes.
Posted 6/11/2026full-timeLa Jolla • California, New York, Pennsylvania, Washington • 🇺🇸 United StatesSenior💰 $139,100 - $231,900 per yearWebsite
About the role
Key responsibilities & impact- Join a team of scientists supporting oncology clinical development programs.
- Serve as the primary Clinical Pharmacology Lead providing expertise.
- Oversee clinical pharmacology studies with operational assistance.
- Direct planning of all relevant PK-PD analyses.
- Provide recommendations for clinical doses and dosing algorithms.
Requirements
What you’ll need- PhD or PharmD.
- 3+ years of related experience.
- Experience applying pharmacokinetic and pharmacokinetic-pharmacynamic concepts, including modeling and simulation to clinical trial design.
- Clinical drug development experience in oncology or other therapeutic area.
- Strong communication skills--written, verbal and presentation.
- Strong technical proficiency with pharmacokinetic software (e.g., WinNonlin, NONMEM, S-Plus, R).
Benefits
Comp & perks- Health benefits to include medical, prescription drug, dental and vision coverage.
- 401(k) plan with Pfizer Matching Contributions.
- Additional Pfizer Retirement Savings Contribution.
- Paid vacation, holiday and personal days.
- Paid caregiver/parental and medical leave.
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
pharmacokineticspharmacodynamicsmodelingsimulationclinical trial designclinical drug developmentdosing algorithmsPK-PD analysis
Soft Skills
communicationwritten communicationverbal communicationpresentation skills
Certifications
PhDPharmD