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Director, Clinical Pharmacology & Pharmacometrics

Portsmouth
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Social network you want to login/join with:Director, Clinical Pharmacology and Pharmacometrics, Portsmouth, Hampshire

Client: Planet PharmaLocation: Portsmouth, Hampshire, United KingdomJob Category:

OtherEU work permit required:

YesJob Views:

3Posted:

22.08.2025Expiry Date:

06.10.2025Job Description:

Clinical Pharmacology and Pharmacometrics Director – Oncology and Neuroscience FocusLocation: England, RemoteFull-Time | Senior-LevelAre 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 RandD 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 DoingLead 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 ForPhD 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 ClientBe 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 ..... full job details .....

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