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Director quantitative pharmacology

Cambridge
Regeneron Pharmaceuticals, Inc
Director
Posted: 23 August
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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.

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