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Manager, Clinical Pharmacology
PfizerClinical Pharmacology Lead providing expertise to oncology project teams at Pfizer. Overseeing pharmacology studies and regulatory contributions for drug development teams.
Posted 7/15/2026full-timeCalifornia, Connecticut, Massachusetts, New York, Washington • 🇺🇸 United StatesMid-LevelSenior💰 $106,000 - $176,600 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Clinical Pharmacology, including pharmacokinetics and pharmacodynamics, with a strong focus on model-based drug development and regulatory compliance. Proficient in executing PK analysis and integrating data into clinical trial designs.
Highest-signal resume keywords
PhD In PharmacokineticsClinical Pharmacology ExpertisePK/PD Data InterpretationModel-Based Drug DevelopmentR, NONMEM, Monolix Proficiency
ATS Keywords
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Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
PharmacokineticsPharmacodynamicsClinical Study ProtocolsPK AnalysisPK/PD AnalysisDosing RegimensQuantitative ApproachesClinical Trial DesignRegulatory Document ContributionOperational Assistance
Soft Skills
Strong Written CommunicationStrong Verbal Communication
Tools & Technologies
RNONMEMMonolix
Certifications & Qualifications
PhD In PharmacokineticsPhD In Clinical PharmacologyPhD In PharmacometricsPhD In EngineeringPharmD
Industry Keywords
Oncology Development ProgramsClinical Pharmacology LeadMultidisciplinary Project TeamsClinical Pharmacology StudiesRegulatory Agencies
About the role
Key responsibilities & impact- Join a team of scientists supporting oncology development programs
- Act as Clinical Pharmacology Lead providing pharmacology expertise to multidisciplinary project teams
- Provide clinical pharmacology components to Clinical Study Protocols, Reports, and plans
- Plan, design, and oversee clinical pharmacology studies with operational assistance
- Implement model-based drug development using quantitative approaches
- Execute PK analysis and conduct appropriate PK/PD analyses
- Integrate knowledge of pharmacokinetics, pharmacodynamics, and patient characteristics to optimize doses
- Provide recommendations for clinical doses and dosing regimens
- Contribute to all regulatory documents and support resolution of queries from drug regulatory agencies
Requirements
What you’ll need- PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD
- Strong written and verbal communication skills
- Experience interpreting PK and PK/PD data and integrating this into clinical trials
- Hands-on experience with common software tools for PK and PK/PD analyses (e.g., R, NONMEM, Monolix)
Benefits
Comp & perks- Comprehensive and generous benefits and programs to help colleagues lead healthy lives
- 401(k) plan with Pfizer Matching Contributions
- Additional 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