Associate Director – Quantitative Pharmacology

Regeneron

. Lead model-informed drug development strategies across therapeutic areas and modalities including antibodies, siRNA, and gene therapies .

Posted 9/23/2026full-timeUnited StatesSenior💰 $176,100 - $287,300 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Expertise in Quantitative Pharmacology and Pharmacometrics, with a strong focus on population PK/PD and exposure–response modeling. Proven ability to lead drug development strategies, mentor junior scientists, and ensure compliance with regulatory standards.

Highest-signal resume keywords

PhD In Quantitative PharmacologyPopulation PK/PD ModelingNONMEM ExperienceRegulatory Submission SupportExceptional Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

PharmacometricsQuantitative PharmacologyExposure–Response ModelingMechanistic ModelingPopulation PK/PDQuantitative AnalysisStatistical Modeling

Soft Skills

Interpersonal SkillsInfluencing SkillsMentoring

Tools & Technologies

NONMEMMonolixSimulxMATLAB/SimbiologyR

Industry Keywords

Drug DevelopmentRegulatory ComplianceFDAEMAPMDA

About the role

Key responsibilities & impact

Lead model-informed drug development strategies across therapeutic areas and modalities including antibodies, siRNA, and gene therapies
Inform dose selection, trial design, and regulatory strategy from early development through submission
Drive model-informed development and pharmacometrics strategies with Clinical Pharmacology, Biostatistics, Clinical, and Translational teams
Lead Quantitative Pharmacology evaluation of assets
Deliver population PK/PD, exposure–response, and translational modeling analyses
Represent Quantitative Pharmacology at program and governance meetings
Communicate quantitative insights to non-modeling audiences
Contribute to regulatory interactions and author Quantitative Pharmacology components of regulatory documents
Mentor and develop junior scientists
Identify and implement process improvements, new modeling approaches, and quantitative tools
Ensure analyses and documentation meet scientific quality and regulatory compliance standards

Requirements

What you’ll need

PhD in Quantitative Pharmacology, Pharmacometrics, Engineering, or a related field with 7+ years of industry experience; or MS with 10+ years of relevant experience
Demonstrated expertise in population PK/PD, exposure–response, or mechanistic modeling (systems biology, or QSP)
Experience using NONMEM, Monolix, Simulx, MATLAB/Simbiology and R
Proven track record of delivering analyses supporting regulatory submissions
Experience engaging directly with agencies such as FDA, EMA, and PMDA
Hands-on experience with a broad range of quantitative and computational tools
Strong publication record
Exceptional communication and interpersonal skills
Ability to influence and partner effectively across technical and non-technical teams

Benefits

Comp & perks

Annual bonuses or other incentive plans
Equity awards
Pension or retirement benefits
401(k) company match
Health and wellness programs
Fitness centers
Medical, dental, vision, life and disability insurance benefits
Paid time off
Family support benefits
Reasonable accommodation during the recruitment process where required