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

Pierre Fabre

Haute Garonne, France
Hybrid (on-site with up to 2 days of teleworking)
Pk/pd and biomarker oversight
Clinical study design support
Sample management oversight
Pierre Fabre is seeking a Clinical Study Monitor focused on pharmacokinetics, pharmacodynamics, and biomarkers to support their clinical research team in Haute Garonne, France. The role requires oversight of clinical trials, ensuring compliance and data integrity, while offering a competitive benefits package and the possibility of teleworking

Job Summary

  • Support Clinical Pharmacology and Biomarker Experts in the design, execution, and analysis of clinical studies within the R&D team.
  • Ensure high-quality operational oversight of PK, PD, and biomarker components within early and late phase clinical trials.
  • This position is compatible with teleworking up to 2 days a week according to company rules.

Matching Summary

Match Score: 85

Pierre Fabre is seeking a Clinical Study Monitor focused on pharmacokinetics, pharmacodynamics, and biomarkers to support their clinical research team in Haute Garonne, France. The role requires oversight of clinical trials, ensuring compliance and data integrity, while offering a competitive benefits package and the possibility of teleworking.

Skills & Requirements

Must-have

  • PK/PD and biomarker oversight
  • Clinical study design support
  • Sample management oversight
  • Bioanalytical activities monitoring
  • Regulatory documentation maintenance
  • Budget tracking and forecasting

Nice-to-have

  • Cross-functional collaboration
  • Proactive problem-solving
  • Attention to quality
  • Team-oriented mindset

Key Requirements

  • Master’s degree in Life Sciences or related field
  • Experience in clinical study conduct
  • Good understanding of GCP
  • Excellent written and verbal communication skills in English

Work Rights

Not specified

Tailored Resume

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