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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical pharmacology, including mechanistic PK/PD modeling and clinical trial simulations. Proficient in designing and executing clinical pharmacology plans while ensuring compliance with regulatory standards.
Highest-signal resume keywords
Clinical Pharmacology ExpertiseMechanistic PK/PD ModelingClinical Trial SimulationsRegulatory Document ContributionExcellent Communication Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
PharmacokineticsPharmacometricsPopulation ModelingNONMEMRClinical Development PlansDose-Range-Finding StrategiesAnalytical MethodsProtocol AuthoringStudy Design Optimization
Soft Skills
LeadershipCollaborationPresentation SkillsInfluencing SkillsGlobal Team Coordination
Certifications & Qualifications
M.D.Ph.D.Pharm.D.
Industry Keywords
Clinical PharmacologyPK/PD AnalysesRegulatory GuidelinesINDsNDAsMAAsSOPsLiterature Meta-AnalysesScientific SocietiesIndustry Consortia
About the role
Key responsibilities & impact- Act as Clinical Pharmacology representative on Clinical Sub Teams, Development Teams, and other multifunctional teams
- Provide clinical pharmacology expertise, leadership, and deliverables for assigned projects
- Design and execute clinical pharmacology plans and implement best practices on project teams
- Collaborate with disciplines to establish preclinical PK/PD knowledge and predictive models before first-in-human studies
- Plan and oversee project-level clinical pharmacology activities, including clinical development plans and PK/PD analyses
- Plan and oversee study-level activities, including protocol authoring, clinical phase oversight, and reporting
- Ensure appropriate dose-range-finding strategies and optimal doses and dosage regimens
- Design and implement end-to-end model-informed drug discovery and development plans
- Use innovative analytical methods to optimize doses, dosage regimens, and study designs
- Contribute to regulatory documents, including briefing documents, regulatory queries, investigator brochures, INDs, and NDAs/MAAs
- Monitor literature, regulatory guidelines, internal guidance, and SOPs
- Influence the external environment through publications, presentations, scientific societies, and industry consortia
Requirements
What you’ll need- Strong quantitative skills and expertise in mechanistic PK/PD modeling/systems pharmacology, literature meta-analyses, population modeling, and clinical trial simulations using NONMEM, R, or similar tools
- M.D./Ph.D., or equivalent training/experience in pharmacokinetics, pharmacometrics, clinical pharmacology, engineering, or a related discipline, with 0+ years of industry experience
- Pharm.D., or equivalent training/experience in pharmacokinetics, pharmacometrics, clinical pharmacology, engineering, or a related discipline, with 2+ years of industry experience
- Excellent written and verbal communication skills
- Demonstrated presentation skills
- Ability to work in global team meetings across different time zones periodically based on business necessity
- Ability to influence and collaborate with peers to achieve meaningful outcomes and create business impact
- Must be authorized to be employed in the U.S. by any employer
- Must have permanent work authorization in the United States
- U.S. work visa sponsorship is not available now or in the future
Benefits
Comp & perks- Global Performance Plan bonus target of 15.0% of base salary
- Share-based long-term incentive program
- 401(k) plan with Pfizer Matching Contributions
- Additional Pfizer Retirement Savings Contribution
- Paid vacation, holiday, and personal days
- Paid caregiver/parental and medical leave
- Medical, prescription drug, dental, and vision coverage
- Relocation assistance may be available based on business needs and/or eligibility
- Employee referral bonus eligibility
