(associate) Clinical Project Manager - Sponsor Dedicated (fixed-term Contract For 6 Months)

IQVIA UK

Paris, France
Clinical trial management experience
Knowledge of gcp and ich guidelines
Fluent in french and english
The role involves managing phase II-III clinical research projects in various therapeutic areas

Job Summary

  • The role involves managing phase II-III clinical research projects in various therapeutic areas.
  • You will ensure compliance with regulatory requirements and maintain high ethical standards.
  • The position offers an opportunity to work closely with a key client in a dynamic environment.

Matching Summary

The role involves managing phase II-III clinical research projects in various therapeutic areas.

Skills & Requirements

Must-have

  • Clinical trial management experience
  • Knowledge of GCP and ICH guidelines
  • Fluent in French and English

Nice-to-have

  • Experience in rare diseases or cardiology
  • Strong problem solving skills
  • Excellent leadership and collaboration skills

Key Requirements

  • Master's or higher-level degree in life science
  • At least 2 years of clinical trial management experience
  • Familiarity with Veeva as CTMS/TMF

Work Rights

Not specified

Tailored Resume

Cover Letter