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.
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 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:
- 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 inc. 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
:quality(80))
:quality(80))
:quality(80))