Alternance Chef De Projets Opérations Cliniques H/f

Mayoly

Paris, France
Clinical trial authorizations
Regulatory dossier preparation
International mother company communication
Participate in the preparation and monitoring of Clinical Trial Authorisation requests and Substantial Modification requests submitted for evaluation to regulatory bodies

Job Summary

  • Participate in the preparation and monitoring of Clinical Trial Authorisation requests and Substantial Modification requests submitted for evaluation to regulatory bodies.
  • Participate in the management and monitoring of the start-up of clinical trials, including regulatory and operational aspects, and the management of the supply of treatments and materials for clinical studies.
  • Develop autonomy in the main activities managed by a clinical research department to facilitate future employability in this field.

Matching Summary

Participate in the preparation and monitoring of Clinical Trial Authorisation requests and Substantial Modification requests submitted for evaluation to regulatory bodies.

Skills & Requirements

Must-have

  • Clinical Trial Authorizations
  • Regulatory Dossier Preparation
  • International Mother Company Communication
  • Clinical Trial Supply Management
  • Cross-departmental Collaboration

Nice-to-have

  • Teamwork and Interpersonal Skills
  • Curiosity and Drive
  • Adaptability and Initiative

Key Requirements

  • Bac + 4/5 in Clinical Research
  • Knowledge of clinical trial regulatory framework
  • Proficiency in Microsoft Office Suite
  • Fluent English (written and oral)

Work Rights

Not specified

Tailored Resume

Cover Letter