Job DescriptionThis 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.We’re looking for an experienced scientist to lead non-clinical PKPD strategy, working across study design, data analysis, and regulatory submissions to help bring new therapies to patients.Responsibilities:Lead design and execution of non-clinical PKPD and GLP toxicokinetics studiesAnalyse data using Phoenix WinNonLin, Berkeley Madonna and RProduce clear reports and regulatory-standard documentationCollaborate with internal teams and CROs to deliver high-quality, compliant dataCommunicate results effectively to scientific and project stakeholdersIdeal Profile:PhD/MSc/BSc in relevant discipline, 5+ years’ PKPD analysis experience in pharma/CROStrong understanding of pharmacology and drug actionProven track record in regulatory-standard study design and reporting inc. strong experience with WinNonLinExcellent communication skills and ability to work in a matrix environmentOrganised, proactive, and able to manage multiple projectsDay 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

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