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PK PD Project Manager- Senior Pharmacokinetics Pharmacodynamics Scientist (M / F) - CDI

Pierre Fabre Group

Occitanie

Hybride

EUR 40 000 - 60 000

Plein temps

Il y a 22 jours

Résumé du poste

A prominent pharmaceutical company in France is seeking a talented PKPD project leader to drive innovative drug development strategies. The ideal candidate will have over 5 years of experience in PKPD and thrive in an international, collaborative environment. This role offers opportunities for teleworking and a comprehensive benefits package including health insurance and profit-sharing.

Prestations

Incentives
Profit-sharing
Health insurance
16 additional holidays (RTT)
Public transport participation

Qualifications

  • At least 5 years of industry experience in drug development.
  • Fluency in English, both written and spoken.
  • Practical knowledge of PK/PKPD trial design and execution.

Responsabilités

  • Define PKPD needs across all development stages.
  • Lead or coordinate PK/PKPD studies, ensuring scientific rigor.
  • Provide PKPD assessments of external assets.

Connaissances

PKPD experience
Scientific acumen
Communication skills
Description du poste
Overview

Your mission

We’re looking for a talented and driven PKPD project leader with a strong background in drug development and a passion for innovation to join our dynamic PKPD department. If you thrive in international, cross-functional environments and want to shape the future of therapeutic discovery, we want to hear from you.

As a key scientific leader and member of the core project teams, you will design and implement cutting-edge PKPD, DMPK, and ADME strategies from early discovery through preclinical development. You’ll be the face of the PKPD department in internal and external engagements—collaborating with global experts, regulatory authorities, and strategic partners.

What You’ll Do
  • Strategic Leadership : Define PKPD needs across all development stages—from early preclinical to First-in-Human—ensuring alignment on study design, timelines, and budgets.
  • Study Oversight : Lead or coordinate in vitro, in vivo, and in silico PK / PKPD studies, whether conducted in-house or outsourced, ensuring scientific rigor and operational excellence.
  • Asset Evaluation : Provide expert PKPD assessments of external assets, contributing to strategic decision-making in licensing or acquisition.
  • Cross-Functional Collaboration : Work closely with clinicians, statisticians, pharmacologists, toxicologists, and regulatory experts to drive project success.
  • Scientific Documentation : Author key sections of regulatory and scientific documents, including study protocols, Investigator’s Brochures (IB), IND / IMPDs, NDAs, PIPs, and Risk Management Plans.
  • Global Engagement : Represent the PKPD function in interactions with regulatory bodies, CROs, key opinion leaders, and business partners.
🌍 What You Bring
  • Proven experience in PKPD within drug development, ideally in an international setting.
  • Strong scientific acumen and ability to translate complex data into actionable insights.
  • Excellent communication skills and a collaborative mindset.

This position is compatible with teleworking up to 2 days a week after the trial period.

We offer an attractive remuneration / benefits package : Incentives, profit-sharing, Pierre Fabre shareholding with matching contribution, health and provident insurance, 16 days of holidays (RTT) in addition to 25 days of personal holidays, public transport participation, very attractive CE...

Who you are ?
  • At least 5 year industry experience in a multicultural English speaking environment, with a solid track record in PK / PKPD drug development
  • Practical knowledge and experience of PK / PKPD preclinical and clinical trial design and execution, including data collection, analysis and reporting approaches + filling of regulatory dossiers.
  • Previous experience (hands-on) interpretation of PK and PKPD data, with in-silico methods.
  • Significant track record with early drug development phases or moving candidate drugs to the clinic.

Fluency in English, both written and spoken.

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