Clinical Study Monitor (pk/pd & Biomarkers Focus)- Cdi- F/m

Pierre Fabre

Toulouse, France
Hybrid (compatible with teleworking up to 2 days a week)
Experience in clinical study conduct
Good understanding of gcp
Strong organizational skills
Pierre Fabre is seeking a Clinical Study Monitor with a focus on pharmacokinetics, pharmacodynamics, and biomarkers to support their clinical research team in Toulouse, France. The ideal candidate will have experience in clinical study conduct and a solid understanding of regulatory documentation processes. The position offers a hybrid work model with attractive benefits including profit-sharing and additional holidays

Job Summary

  • We are seeking a Clinical Study Monitor to support Clinical Pharmacology and Biomarker Experts.
  • This role ensures high-quality operational oversight of PK, PD, and biomarker components within clinical trials.
  • We offer an attractive remuneration and benefits package including health insurance and additional holidays.

Matching Summary

Match Score: 85

Pierre Fabre is seeking a Clinical Study Monitor with a focus on pharmacokinetics, pharmacodynamics, and biomarkers to support their clinical research team in Toulouse, France. The ideal candidate will have experience in clinical study conduct and a solid understanding of regulatory documentation processes. The position offers a hybrid work model with attractive benefits including profit-sharing and additional holidays.

Skills & Requirements

Must-have

  • Experience in clinical study conduct
  • Good understanding of GCP
  • Strong organizational skills

Nice-to-have

  • Proficiency in pharmacokinetic data analysis software
  • Excellent written and verbal communication skills
  • Team-oriented mindset

Key Requirements

  • Master’s degree in Life Sciences or related field
  • Experience with regulatory documentation
  • Prior interaction with CROs preferred

Work Rights

Not specified

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