Alternance Chef De Projets Opérations Cliniques H/f

MOBS Lab

Paris, France
Clinical trial documentation
Regulatory framework knowledge
Cross-functional collaboration
Participate in the preparation and follow-up of Clinical Trial Authorisation applications and Substantial Modification requests submitted to regulatory authorities

Job Summary

  • Participate in the preparation and follow-up of Clinical Trial Authorisation applications and Substantial Modification requests submitted to regulatory authorities.
  • Collaborate closely with clinical research teams and potentially conduct site visits to meet clinical investigation site teams.
  • Develop autonomy in key clinical research activities to facilitate future employability in the field.

Matching Summary

Participate in the preparation and follow-up of Clinical Trial Authorisation applications and Substantial Modification requests submitted to regulatory authorities.

Skills & Requirements

Must-have

  • Clinical Trial Documentation
  • Regulatory Framework Knowledge
  • Cross-functional Collaboration
  • International Team Communication
  • Clinical Trial Supply Management

Nice-to-have

  • Dynamic and Challenging Environment
  • Teamwork and Interpersonal Skills
  • Curiosity and Drive
  • Autonomy and Rigor

Key Requirements

  • Bac +4/5 in Clinical Research
  • 12-24 month internship duration
  • Proficiency in English (written and oral)
  • Proficiency in Microsoft Office Suite

Work Rights

Not specified

Tailored Resume

Cover Letter