OverviewPrincipal Recruitment Consultant at VRS - Analytical Chemistry | Life Science | Synthetic Organic Chemistry

This is an opportunity to join a successful biopharmaceutical company, delivering novel solutions to a range of disease areas. Using integrated PKPD, modelling, and DMPK approaches you will drive smarter drug development — from target ID to first in human clinical trials.

Responsibilities

Lead design and execution of non-clinical PKPD and GLP toxicokinetics studies

Analyse data using Phoenix WinNonLin, Berkeley Madonna and R

Produce clear reports and regulatory-standard documentation

Collaborate with internal teams and CROs to deliver high-quality, compliant data

Communicate results effectively to scientific and project stakeholders

Ideal Profile / Qualifications

PhD/MSc/BSc in relevant discipline, 5+ years’ PKPD analysis experience in pharma/CRO

Strong understanding of pharmacology and drug action

Proven track record in regulatory-standard study design and reporting incl. strong experience with WinNonLin

Excellent communication skills and ability to work in a matrix environment

Organised, proactive, and able to manage multiple projects

Day to day responsibilities can be carried out either onsite or at home with a requirement for the job holder to be onsite at least 2 days/week.

The role is offered on an initial 12 month contract basis with realistic potential for extension.

Apply to VRS today!

Keywords: PK, PD, pharmacokinetics, pharmacodynamics, pharmacology, DMPK, metabolism, pharmaceutical, toxicology, WinNonLin, Berkshire, Reading, Slough, London,

VRS9114SE

Seniority level

Mid-Senior level

Employment type

Contract

Job function

Science and Project Management

Industries

Biotechnology Research and Pharmaceutical Manufacturing

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