Clinical Research Associate - Iqvia Biotech (homebased In Paris)

IQVIA UK

Paris, France
Site monitoring visits execution
Good clinical practice (gcp) adherence
Subject recruitment plan tracking
The role involves partnering with biotech companies to accelerate clinical development from early phase through global registrational studies

Job Summary

  • The role involves partnering with biotech companies to accelerate clinical development from early phase through global registrational studies.
  • Candidates must perform comprehensive site monitoring visits while ensuring strict adherence to Good Clinical Practice and ICH guidelines.
  • The position requires managing study progress by tracking regulatory submissions, enrollment, and resolving data queries effectively.

Matching Summary

The role involves partnering with biotech companies to accelerate clinical development from early phase through global registrational studies.

Skills & Requirements

Must-have

  • Site monitoring visits execution
  • Good Clinical Practice (GCP) adherence
  • Subject recruitment plan tracking
  • Trial Master File maintenance
  • Protocol training administration

Nice-to-have

  • Oncology therapy area experience
  • Effective time management skills
  • Strong problem-solving abilities
  • Financial management of sites
  • Collaborative team relationship building

Key Requirements

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

Work Rights

Must be based in commutable distance to Paris

Tailored Resume

Cover Letter