Associate Director Quantitative Pharmacology

We are seeking a highly motivated Associate Director to join the Quantitative Pharmacology (QP) group. The Associate Director will lead model-informed drug development strategies supporting one or more therapeutic areas across modalities including antibodies siRNA and gene therapies. This role combines scientific depth with cross-functional leadership to inform dose selection trial design and regulatory strategy from early development through submission.

When & where:

• Work Location: Tarrytown NY Warren NJ and Cambridge MA

• Hybrid: 4 days per week on site

Discover your role:

• 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 Quantitative Pharmacology evaluation of one or more assets accountable for timely delivery of population Pharmacokinetics/Pharmacodynamics exposureresponse and translational modeling analyses.

• Representing Quantitative Pharmacology 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 Quantitative Pharmacology(e.g. Investigators Brochure 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.

This role requires:

• 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 Pharmacokinetics/Pharmacodynamics (PK/PD) exposureresponse or mechanistic modeling (systems biology or

  Quantitative Systems Pharmacology ) 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.

• Exceptional communication and interpersonal skills with the ability to influence and partner effectively across technical and non-technical teams.

Does this sound like you Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race color religion or belief (or lack thereof) sex sexual orientation gender identity or expression gender reassignment marital or civil partnership status civil status pregnancy or parental status age disability nationality citizenship status ethnic or national origin membership of the Traveler community familial status genetic information military or veteran status or any other characteristic protected under applicable law. Where required we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process unless such accommodation would impose undue hardship.

Where necessary we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment specific role level and your skills and some countries collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include depending on country and role: annual bonuses or other incentive plans equity awards pension or retirement benefits 401(k) company match health and wellness programs fitness centers insurance benefits (e.g. medical dental vision life and disability) paid time off and family support benefits. For additional information about Regeneron benefits in the U.S. please visit For other locations additional information will be provided during the recruitment process. If you have any questions please speak with your recruiter.

Please be advised that at Regeneron we believe we do our best work when we are together. For that reason many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.

As part of the recruitment process certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)