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Principal Scientist - Non-clinical PKPD

Hays Specialist Recruitment Limited
Posted 16 days ago, valid for 3 days
Location

Slough, Berkshire SL13XX, England

Contract type

Full Time

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Sonic Summary

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  • A leading global biopharmaceutical company in Slough is seeking a Principal Scientist for a 12-month contract in their Non-Clinical PK/PD team.
  • The role involves designing and executing non-clinical PK/PD and GLP toxicokinetic studies, contributing to drug development from target identification to life cycle management.
  • Candidates need a PhD or MSc in quantitative pharmacology, pharmacokinetics/pharmacodynamics, or a related field, along with significant hands-on experience in PK/PD.
  • Proficiency in Phoenix WinNonlin for PK/PD analysis is essential, and a strong understanding of pharmacology and disease-related drug mechanisms is required.
  • The salary for this position is competitive, reflecting the candidate's experience and expertise in the field.

Your new companyYou will be joining a leading global biopharmaceutical company based in Slough who are looking for a Principal Scientist to join their Non-Clinical PK/PD team within Early Clinical Development & Translational Sciences. This contract role (12 months) focusses on the design and execution of non-clinical PK/PD and GLP toxicokinetic (TK) studies, playing a key role in shaping pharmacokinetic and pharmacology strategies.The successful candidate will contribute to DMPK and PK/PD activities across the drug development continuum, from target identification through to life cycle management, supporting the advancement of innovative therapeutic programmes.Your new role

  • Lead the design and execution of non-clinical PK/PD and GLP toxicokinetic studies, shaping and driving the overall non-clinical pharmacokinetic/pharmacodynamic (PK/PD) strategy.
  • Contribute to the development of study protocols, including regulatory and exploratory designs, to support the progression of innovative therapeutic candidates.
  • Collaborate cross-functionally with internal and external teamsto gather requirements, align objectives, and ensure timely delivery of project milestones.
  • Advance drug development efforts by applying deep expertise in drug pharmacology and PK/PD to inform decision-making and optimise candidate selection.
  • Serve as a key liaison between stakeholders, effectively representing departmental interests and ensuring alignment with broader organisational goals.

What you'll need to succeed

  • A PhD or MSc (or equivalent experience) in quantitative pharmacology, pharmacokinetics /pharmacodynamics, DMPK, biology or a related discipline, with strong hands-on experience in PK/PD within a pharmaceutical, biotech, CRO or consultancy environment.
  • Proven expertise in non-clinical PK/PD study design, data analysis, and regulatory reporting, with a strong understanding of pharmacology and disease-related drug mechanisms.
  • Demonstrated hands-on experience in generating and interpreting high-quality preclinical PK/PD data to support drug development.
  • Proficiency in Phoenix WinNonlin for PK/PD analysis is essential; experience with additional modelling and simulation tools such as Berkeley Madonna and/or R is highly desirable.
  • A track record of scientific publications and contributions relevant to PK/PD is considered an asset.

What you'll get in returnThe chance to make a significant impact on the company's portfolio and work within a highly experienced team.What you need to do nowIf you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.Keywords: Principal, Scientist, Nonclinical, PKPD, Pharmacokinetics, Pharmacodynamics, PK, PD, Toxicokinetics, GLP, Compliance, Phoenix, WinNonlin, Berkeley, Madonna, R, Programming, Quantitative, Pharmacology, DMPK, Drug, Development, Preclinical, Translational, biotech, pharma, Clinical, Bioanalysis, Immunogenicity, Safety, Regulatory

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

SonicJobs' Terms & Conditions and Privacy Policy also apply.