Chargé De Développement Clinique - Tous Genres

Biocodex

Compiègne, France
Clinical development strategy
Regulatory affairs alignment
Scientific data analysis
You will play a key role as an interface between Global Medical Affairs, Global Pharma & Regulatory Affairs, and the Clinical Operations team, contributing to the alignment between scientific strategy, regulatory requirements, and the execution of clinical development programs

Job Summary

  • You will play a key role as an interface between Global Medical Affairs, Global Pharma & Regulatory Affairs, and the Clinical Operations team, contributing to the alignment between scientific strategy, regulatory requirements, and the execution of clinical development programs.
  • You will contribute to the design and development of new health products (food supplements, medical devices, medicines, or others), and follow up on investigator-initiated clinical studies.
  • Biocodex offers a CDI contract, Cadre status, a site in Compiègne (Oise), and benefits including I/P, teleworking, and social works.

Matching Summary

You will play a key role as an interface between Global Medical Affairs, Global Pharma & Regulatory Affairs, and the Clinical Operations team, contributing to the alignment between scientific strategy, regulatory requirements, and the execution of clinical development programs.

Skills & Requirements

Must-have

  • Clinical development strategy
  • Regulatory affairs alignment
  • Scientific data analysis
  • Clinical study protocols
  • Investigator-initiated studies
  • Scientific and regulatory watch

Nice-to-have

  • Teamwork and transversal collaboration
  • Innovation and performance focus
  • Commitment to diversity and inclusion
  • Holistic CSR approach

Key Requirements

  • Scientific degree (Doctorate or Master)
  • Proven experience in clinical development
  • Proficiency in Office tools
  • Proficiency in English
  • Operational project execution

Work Rights

Not specified

Tailored Resume

Cover Letter