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Director, clinical pharmacology & pharmacometrics

Telford
Jr United Kingdom
Director
Posted: 24 August
Offer description

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Director, Clinical Pharmacology & Pharmacometrics, Telford

Client:

Planet Pharma

Location:

Telford, United Kingdom


Job Category:

Other


EU work permit required:

Yes


Job Views:

3


Posted:

22.08.2025


Expiry Date:

06.10.2025


Job Description:

Clinical Pharmacology & Pharmacometrics Director – Oncology & Neuroscience Focus

Location: England, Remote

Full-Time | Senior-Level

Are you ready to make a meaningful impact in the lives of patients with serious medical conditions? A leading global biopharma company is seeking an experienced and innovative Clinical Pharmacology Lead to join its growing R&D team. This is a unique opportunity to work across multiple therapeutic areas, including oncology, neuroscience, and rare diseases, helping bring cutting-edge therapies from early discovery through to late-stage clinical trials and commercialization.

What You'll Be Doing

* Lead the clinical pharmacology strategy across multiple programs from preclinical candidate nomination through to phase 4 studies.
* Design and support PK/PD studies, contribute to clinical protocol development (Phase 1–4), and analyze pharmacokinetic and pharmacodynamic data.
* Serve as the subject matter expert in cross-functional teams, owning dose selection strategy and regulatory justification.
* Collaborate closely with pharmacometrics, clinical, regulatory, and external partners to enable smart, data-driven decisions.
* Contribute to regulatory submissions (INDs, NDAs/BLAs) and address agency questions with confidence and clarity.
* Support scientific publications and conference presentations to share ground-breaking insights.

What We’re Looking For

* PhD or MD with substantial industry experience in clinical pharmacology, PK/PD, or pharmacometrics.
* Strong understanding of drug development across all clinical phases.
* Proficiency in tools such as Phoenix WinNonlin, R, NONMEM, or similar for pharmacokinetic modeling and analysis.
* Demonstrated success in regulatory submissions and interactions with global health authorities.
* A proactive, collaborative mindset, with the ability to lead and contribute in cross-functional environments.
* Excellent communication and presentation skills, both written and verbal.

Why Join Our Client

* Be part of a science-driven, patient-focused organization committed to transforming lives.
* Work on innovative programs with real-world impact, including therapies for underserved conditions.
* Join a supportive, high-performing team that values curiosity, integrity, and collaboration.
* Competitive compensation, flexible working model, and career growth opportunities in an international setting.
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