Clinical Research Associate - Iqvia Biotech (homebased In Paris)

IQVIA

Paris, France
Good clinical practice gcp compliance
Ich guidelines adherence
Site monitoring visits execution
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines

Job Summary

  • The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines.
  • Candidates will work directly with clinical sites to adapt and drive subject recruitment plans to enhance predictability for project needs.
  • IQVIA Biotech partners with visionary biotech companies to accelerate clinical development from early phase through global registrational studies.

Matching Summary

The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines.

Skills & Requirements

Must-have

  • Good Clinical Practice GCP compliance
  • ICH guidelines adherence
  • Site monitoring visits execution
  • Subject recruitment plan tracking
  • Trial Master File maintenance

Nice-to-have

  • Oncology therapeutic area experience
  • Strong problem-solving skills
  • Effective time management abilities
  • Financial management of sites
  • Collaborative team communication

Key Requirements

  • Minimum 1 year monitoring experience
  • Bachelor's degree in scientific discipline
  • Background in Life Science or Nursing
  • Previous Study Coordinator experience preferred

Work Rights

Must be based in commutable distance to Paris

Tailored Resume

Cover Letter