Director Quantitative Pharmacology

Regeneron Pharmaceuticals, Inc; Cambridge; On-site; GBP 90,000 - 120,000; Full time

Job summary

A leading biopharmaceutical company in Cambridge is seeking a Director of Quantitative Pharmacology to deliver quantitative analysis and support R&D programs. The ideal candidate will have a PhD and over 8 years of experience, with strong regulatory interaction and a solid publication record. This role demands proficiency in pharmacokinetic and pharmacodynamic principles, along with leadership in complex projects.

Qualifications

• Comprehensive knowledge of pharmacokinetic/pharmacodynamic principles, pharmacology, biology, and drug development.
• Deep understanding of scientific literature and technical PK/PD skills.
• Recognized as an expert in your field.
• Extensive regulatory experience, including authoring regulatory documents.

Responsibilities

• Accountable for PK/PD evaluation of a portfolio of products.
• Deliver timely and accurate quantitative analyses and reports.
• Inform management of program and regulatory developments.
• Ensure high quality and accuracy in analyses and documentation.

Skills

Pharmacokinetic principles

Pharmacodynamic principles

Regulatory experience

Quantitative analysis

Communicating complex information

Education

PhD in Quantitative Pharmacology or related field

Job description

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Director Quantitative Pharmacology, Cambridge

Client:

Location: Cambridge, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference:

26058dba7750

Job Views:

26

Posted:

12.08.2025

Expiry Date:

26.09.2025

Job Description:

As a Director in Pharmacometrics (Quantitative Pharmacology), this individual is accountable for supporting one or more research & development programs within their pharmacometrics discipline. The Director is responsible for delivering timely and accurate quantitative analyses, interpretation, and messaging to PMx management, as well as producing well-constructed reports for review.

Typical responsibilities include:

• Managing and being accountable for PK/PD evaluation of a small portfolio of products or projects.
• Working independently, with guidance only in complex situations.
• Informing PMx management of important program and regulatory developments.
• Ensuring analyses and documentation are of high quality and accuracy.
• Developing reports with appropriate messaging and a clear storyline.
• Ensuring reports are suitable for review by senior management.
• Solving complex problems and identifying broad solutions.
• Maintaining a strong publication record and publishing in scientific literature.
• Contributing to multidisciplinary meetings with cross-functional insights.
• Communicating complex information clearly and effectively.

This role may be suitable if you:

• Have comprehensive knowledge of pharmacokinetic/pharmacodynamic principles, pharmacology, biology, and drug development.
• Possess deep understanding of scientific literature and technical PK/PD skills.
• Are recognized as an expert in your field.
• Have extensive regulatory experience, including authoring regulatory documents and engaging with health authorities.

To qualify, you must have a PhD +8 years in Quantitative Pharmacology or a related field, with hands-on experience using quantitative tools, a strong publication record, and proven regulatory interaction experience.