Director Quantitative Pharmacology
Regeneron
June 29, 2026
On-site
Tarrytown, NY
Clinical Research and Development
Responsibilities:
- Deliver pharmacometrics support for one or more R&D programs.
- Provide timely and accurate quantitative analyses, interpretation, and messaging to PMx management.
- Produce well-constructed, well-messaged reports for PMx review.
- Manage PK/PD evaluation for a small portfolio of products or projects.
- Independently handle most matters; seek guidance only in the most complex situations.
- Inform PMx management of important program and regulatory developments.
- Ensure highest quality and accuracy of analyses and documentation.
- Develop appropriate messaging and a meaningful story-line for reports and documents.
- Ensure study reports and other documents undergo appropriate functional review and are suitable for senior management.
- Solve complex problems using a broad perspective.
- Contribute to multi-disciplinary meetings; share cross-functional skills and knowledge.
Qualifications:
- PhD with 8+ years’ experience in Quantitative Pharmacology (pharmacometrics) or a related field.
- Strong knowledge of pharmacokinetic/pharmacodynamic principles, pharmacology/biology, and quantitative aspects of drug development; advanced knowledge of pharmaceutical drug development.
- Deep understanding of scientific literature and technical skills in PK/PD methods.
- Recognized expert in own area within the organization.
- Extensive regulatory experience (e.g., regulatory briefing books, CTD summaries, HA meeting contributions/negotiations, support for BLA or equivalent).
Required/Preferred Skills:
- Hands-on usage of a broad range of quantitative tools and systems.
- Strong publication record in the field.
- Excellent written and oral communication; ability to communicate complex information succinctly.
- Proven experience developing QP elements of regulatory strategy and interacting with regulatory agencies without supervision.
Application Instructions:
- Apply now.
- Deliver pharmacometrics support for one or more R&D programs.
- Provide timely and accurate quantitative analyses, interpretation, and messaging to PMx management.
- Produce well-constructed, well-messaged reports for PMx review.
- Manage PK/PD evaluation for a small portfolio of products or projects.
- Independently handle most matters; seek guidance only in the most complex situations.
- Inform PMx management of important program and regulatory developments.
- Ensure highest quality and accuracy of analyses and documentation.
- Develop appropriate messaging and a meaningful story-line for reports and documents.
- Ensure study reports and other documents undergo appropriate functional review and are suitable for senior management.
- Solve complex problems using a broad perspective.
- Contribute to multi-disciplinary meetings; share cross-functional skills and knowledge.
Qualifications:
- PhD with 8+ years’ experience in Quantitative Pharmacology (pharmacometrics) or a related field.
- Strong knowledge of pharmacokinetic/pharmacodynamic principles, pharmacology/biology, and quantitative aspects of drug development; advanced knowledge of pharmaceutical drug development.
- Deep understanding of scientific literature and technical skills in PK/PD methods.
- Recognized expert in own area within the organization.
- Extensive regulatory experience (e.g., regulatory briefing books, CTD summaries, HA meeting contributions/negotiations, support for BLA or equivalent).
Required/Preferred Skills:
- Hands-on usage of a broad range of quantitative tools and systems.
- Strong publication record in the field.
- Excellent written and oral communication; ability to communicate complex information succinctly.
- Proven experience developing QP elements of regulatory strategy and interacting with regulatory agencies without supervision.
Application Instructions:
- Apply now.