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Regeneron

Associate Director, Quantitative Pharmacology

Regeneron

Associate Director leading model-informed drug development strategies for therapeutic areas at Regeneron. Collaborating cross-functionally to inform regulatory strategy from development through submission.

Posted 5/31/2026full-timeRemote • New York • 🇺🇸 United StatesSenior💰 $176,100 - $287,300 per yearWebsite

About the role

Key responsibilities & impact
  • Leading model-informed drug development strategies supporting one or more therapeutic areas across modalities including antibodies, siRNA, and gene therapies.
  • Driving model-informed development (MIDD) and pharmacometrics strategies in partnership with Clinical Pharmacology, Biostatistics, Clinical and Translational teams to support regulatory and clinical decision-making.
  • Leading the QP evaluation of one or more assets, accountable for timely delivery of population PK/PD, exposure–response, and translational modeling analyses.
  • Representing QP at program and governance meetings, communicating quantitative insights clearly to non-modeling audiences.
  • Contributing to regulatory interactions and authoring key components of regulatory documents related to QP (e.g., IB, briefing books, etc.).
  • Mentoring and developing junior scientists and fostering a culture of scientific rigor and collaboration.
  • Identifying and implementing process improvements, new modeling approaches, and innovative quantitative tools to enhance efficiency and impact.
  • Ensuring analyses and documentation are of the highest scientific quality and regulatory compliance.

Requirements

What you’ll need
  • PhD in Quantitative Pharmacology, Pharmacometrics, Engineering, or a related field with 6+ years of post-doctoral or industry experience; or MS with 9+ years of relevant experience.
  • Demonstrated expertise in population PK/PD, exposure–response, or mechanistic modeling (systems biology, or QSP) using tools such as NONMEM, Monolix, Simulx, MATLAB/Simbiology and R.
  • Proven track record of delivering analyses supporting regulatory submissions and engaging directly with agencies (e.g., FDA, EMA, PMDA).
  • Hands-on experience with a broad range of quantitative and computational tools and a strong publication record.

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

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Hard Skills & Tools
population PK/PDexposure–response modelingmechanistic modelingsystems biologyQSPmodel-informed drug developmentpharmacometricsquantitative analysisregulatory submissionsscientific documentation
Soft Skills
leadershipcommunicationmentoringcollaborationprocess improvementscientific rigor
Certifications
PhD in Quantitative PharmacologyPhD in PharmacometricsPhD in EngineeringMS in related field