Director Quantitative Pharmacology

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

Job summary

A leading biopharmaceutical company in Cambridge seeks a Director of Quantitative Pharmacology. The role involves overseeing quantitative analyses, engaging in regulatory strategies, and maintaining high-quality documentation and communications. Ideal candidates boast a PhD and robust experience within pharmacometrics, with a focus on impactful scientific contributions.

Qualifications

• PhD with 8+ years in Quantitative Pharmacology or a related field.
• Experience with regulatory strategies and agency interactions.
• Strong publication record in scientific literature.

Responsibilities

• Managing PK/PD evaluation for product portfolio.
• Delivering accurate quantitative analyses and reports.
• Interacting with PMx management regarding regulatory developments.

Skills

Interpersonal skills

Communication skills

Problem solving

Quantitative analysis

Education

PhD in Quantitative Pharmacology or related field

Tools

Quantitative tools and systems

Job description

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Director Quantitative Pharmacology, Cambridge

Location: Cambridge, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: 26058dba7750

Job Views: 3

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.

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 high quality and accurate analyses and documentation.
• Developing meaningful messaging and storylines in reports.
• Ensuring reports are suitable for review by senior management.
• Solving complex problems with a broad perspective.
• Maintaining a strong publication record in scientific literature.
• Contributing to multidisciplinary meetings with cross-functional skills.
• Demonstrating excellent interpersonal and communication skills, both written and oral.

Ideal candidate:

• Fully knowledgeable of pharmacokinetic/pharmacodynamic principles, pharmacology, biology, and quantitative drug development aspects.
• Deep understanding of scientific literature and technical PK/PD skills.
• Recognized as an expert in the field within the organization.
• Extensive regulatory experience, including authoring briefing books, CTD summaries, and engaging with health authorities.

Qualifications:

• PhD with 8+ years in Quantitative Pharmacology or a related field.
• Hands-on experience with quantitative tools and systems.
• Strong publication record.
• Excellent interpersonal and communication skills.
• Experience developing regulatory strategies and interacting with agencies independently.