FREE ACCESS
5,000–10,000 jobs/day

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.

Associate Director, Clinical Pharmacology
RegeneronAssociate Director in Clinical Pharmacology at Regeneron focusing on PMx contributions to R&D programs. Leading complex analysis plans and regulatory documentation with a PhD and 6 years experience.
Posted 5/21/2026full-timeTarrytown • New York • 🇺🇸 United StatesSenior💰 $176,100 - $287,300 per yearWebsite
About the role
Key responsibilities & impact- proactively identify and provide significant Pharmacometrics (PMx) contributions
- address strategically important program needs for research and development programs
- communicate complex PMx strategies and results to the development team
- independently design, conduct and oversee PMx analysis plans
- author PMx contributions to regulatory documentation
- perform additional analyses to support regulatory interactions
- draft and review documentation for accuracy, clarity and messaging
- work directly with development or Research teams on PMx elements of program strategy
- contribute to the drafting of PMx program strategies to support standard programs
- support a study team on PMx deliverables and objectives
Requirements
What you’ll need- A PhD in Biology, Pharmacology, Engineering or a Pharmacy (Pharm.D.), Medicine (MD) degree
- at least 6 years of relevant Clinical Pharmacology experience
- understanding of PMx concepts and techniques (advanced pharmacokinetics, advanced pharmacological principles, non-compartmental analysis methods, compartmental modeling, translational modelling/pharmacology, Exposure-Responses analysis methods, Nonlinear Mixed Effects modeling, logistic regression, survival analysis, Bayesian approaches, disease modelling/QSP)
- knowledge of innovative PMx methodologies applicable to clinical trials (survival analysis, stratified or covariate analyses, and strategies for handling missing data)
- good regulatory experience (authoring of regulatory briefing books, CTD summaries, contribution at HA meetings, HA negotiations through regulatory review and approval of BLA or equivalent)
- ability to formulate PMx objectives, design, and analyses for complex clinical projects
- proficient in MS-Excel, R, R-Studio, Phoenix WinNonlin, NLME, NonMem, STAN
Benefits
Comp & perks- health and wellness programs (including medical, dental, vision, life, and disability insurance)
- fitness centers
- 401(k) company match
- family support benefits
- equity awards
- annual bonuses
- paid time off
- paid leaves (e.g., military and parental 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
Pharmacometricsadvanced pharmacokineticsadvanced pharmacological principlesnon-compartmental analysis methodscompartmental modelingtranslational modellingExposure-Responses analysis methodsNonlinear Mixed Effects modelinglogistic regressionsurvival analysis
Soft Skills
communicationindependent designoversightaccuracyclaritymessagingstrategic thinkingcollaborationproblem-solvingformulation of objectives
Certifications
PhD in BiologyPhD in PharmacologyPhD in EngineeringPharm.D.MD