Clinical Study Coordinator - Cdi- H/f

Pierrefabrepharmaceuticals

Toulouse, 31, France
Base: not specified; bonus/equity: incentives + pr...
Clinical trial coordination
Gcp compliance
Trial master file management
The Clinical Study Coordinator will participate in managing clinical trials, supporting the Clinical Study Manager, and ensuring compliance with GCP and company ethical rules

Job Summary

  • The Clinical Study Coordinator will participate in managing clinical trials, supporting the Clinical Study Manager, and ensuring compliance with GCP and company ethical rules.
  • The role offers an attractive remuneration package including incentives, profit-sharing, employee shareholding, health insurance, and additional holidays.
  • Pierre Fabre is a leading dermo-cosmetics and pharmaceutical group recognized for sustainability and ranked among the world's best employers.

Matching Summary

The Clinical Study Coordinator will participate in managing clinical trials, supporting the Clinical Study Manager, and ensuring compliance with GCP and company ethical rules.

Salary

Base: Not specified; Bonus/Equity: Incentives and profit-sharing; Benefits: Health and provident insurance, employee shareholding, holidays, public transport participation

Skills & Requirements

Must-have

  • Clinical trial coordination
  • GCP compliance
  • Trial Master File management
  • Clinical trial document drafting
  • Budget monitoring for clinical trials
  • English fluency

Nice-to-have

  • Oncology knowledge
  • Experience with Veeva TMF solution
  • CRO oversight
  • Regulatory and administrative document development
  • Teleworking up to 2 days a week

Key Requirements

  • Bachelor’s degree or equivalent
  • Specialized training as Clinical Research Associate or health-related field
  • At least 5 years clinical research experience
  • Fluency in spoken and written English

Work Rights

Not specified

Tailored Resume

Cover Letter