Principal Scientist – Non-Clinical PKPD (Contract)UK (Slough-based, VDI only – remote access provided) | 12-month contract |Full-time (37.5 hrs/week) | £35.20–£47.92/hr (PAYE/LTD/Umbrella)We are supporting a global biopharma organisation seeking an experienced

Principal Scientist, Non-Clinical PKPD

to join their

Early Clinical Development and Translational Sciences

group on a

12-month contract .This role sits within the

Quantitative Clinical Pharmacology

function, which integrates PK/PD, systems modelling, clinical pharmacology, and DMPK approaches across the full drug development lifecycle. The position offers an excellent opportunity for a skilled pharmacokinetics/pharmacodynamics scientist to contribute to innovative drug development projects from preclinical through regulatory submission.Key Responsibilities

Lead strategy and execution of non-clinical PKPD and GLP toxicokinetic studies.

Provide scientific input into study protocols and regulatory study designs.

Collaborate cross-functionally with Non-Clinical Safety, Bioanalysis, Clinical Pharmacology, and external CRO partners.

Ensure delivery of high-quality data packages that meet GLP and regulatory submission standards.

Analyse, interpret, and report PKPD/toxicokinetic study results; deliver reports and summaries for regulatory submissions.

Effectively communicate interim and final results to project teams and stakeholders.

Represent the function internally and externally, contributing to scientific reputation and best practices.

Candidate Profile

PhD, MSc, or BSc in pharmacology, quantitative pharmacology, pharmacokinetics/pharmacodynamics, DMPK, or related field.

5+ years’ hands-on PKPD data analysis experience

within pharma or CRO environments.

Strong knowledge of pharmacology and drug mechanisms.

Proven ability to design and deliver non-clinical PKPD studies and GLP toxicokinetics reports.

Proficiency with Phoenix WinNonlin

is essential; experience with modelling/simulation tools (e.g., Berkeley Madonna, R) a plus.

Track record of regulatory submissions and/or scientific publications desirable.

Strong communication skills with the ability to influence and collaborate in a matrix environment.

Contract Details

Duration:

12 months (potential extension).

Hours:

37.5 per week (7.5 per day).

Location:

UK-based; virtual desktop infrastructure (VDI only). Candidate provides own equipment. Future office relocation to Surrey anticipated in 2026/27.

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