Director Quantitative Pharmacologist

Regeneron Pharmaceuticals, Inc; Cambridge; On-site; GBP 80,000 - 120,000; Full time

Job summary

A leading company in the pharmaceutical sector seeks a Director in Quantitative Pharmacology to support research and development programs. This role requires extensive expertise in PK/PD principles and regulatory experience, alongside strong analytical and communication skills, to effectively manage and deliver quantitative analyses for project success.

Qualifications

• PhD +8 years in Quantitative Pharmacology or related field.
• Hands-on experience with quantitative tools.
• Proven publication record and regulatory strategy development.

Responsibilities

• Manage PK/PD evaluation of product portfolio.
• Ensure high-quality analyses and documentation.
• Communicate complex information effectively.

Skills

Pharmacokinetic/Pharmacodynamic principles

Pharmacology

Biology

Drug Development

Regulatory Experience

Education

PhD in Quantitative Pharmacology or related field

Tools

Quantitative tools and systems

Job description

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Director Quantitative Pharmacologist, Cambridge

Client:

Location: Cambridge, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: 0c70d3e55f07

Job Views: 5

Posted: 29.06.2025

Expiry Date: 13.08.2025

Job Description:

As a Director in Pharmacometrics (Quantitative Pharmacology), this individual is accountable for supporting research & development programs within their pharmacometrics discipline. The Director ensures the timely and accurate delivery of quantitative analyses, interpretation, messaging to PMx management, and well-constructed reports for review.

Key responsibilities include:

• Managing and being accountable for PK/PD evaluation of a 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 meaningful storylines.
• Ensuring reports and documents are suitable for review by senior management.
• Solving complex problems with a broad perspective.
• Maintaining a strong publication record in scientific literature.
• Sharing cross-disciplinary skills and knowledge in meetings.
• Communicating complex information clearly and effectively.

This role may be suitable if you:

• Have extensive knowledge of pharmacokinetic/pharmacodynamic principles, pharmacology, biology, and drug development.
• Possess deep understanding of scientific literature and technical skills in PK/PD methods.
• Are recognized as an expert in your area.
• Have regulatory experience, including authoring briefing books, summaries, and participating in regulatory meetings and negotiations.

Qualifications:

• PhD +8 years in Quantitative Pharmacology or related field.
• Hands-on experience with a broad range of quantitative tools and systems.
• Proven publication record and experience in developing regulatory strategies and interacting with agencies.