Experienced Clinical Research Associate, France Based

IQVIA Inc

France
**
Good clinical practice gcp knowledge
International conference on harmonization ich guidelines
Site monitoring visit execution
** IQVIA Inc is seeking an Experienced Clinical Research Associate based in France to perform site monitoring and management tasks for clinical studies. The role requires at least one year of on-site monitoring experience and knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. **

Job Summary

  • The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements.
  • Candidates must work with sites to adapt and track subject recruitment plans to enhance predictability and project success.
  • The position requires maintaining the Investigator's Site File and ensuring all study documents are available for filing in the Trial Master File.

Matching Summary

Match Score: 75

** IQVIA Inc is seeking an Experienced Clinical Research Associate based in France to perform site monitoring and management tasks for clinical studies. The role requires at least one year of on-site monitoring experience and knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. **

Skills & Requirements

Must-have

  • Good Clinical Practice GCP knowledge
  • International Conference on Harmonization ICH guidelines
  • Site monitoring visit execution
  • Subject recruitment plan management
  • Trial Master File maintenance

Nice-to-have

  • Strong organizational and problem-solving skills
  • Effective time and financial management
  • Ability to establish client relationships

Key Requirements

  • At least 1 year of on-site monitoring experience
  • High School Diploma or Degree in scientific discipline
  • Proficiency in Microsoft Word, Excel, and PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter