Clinical Research Associate - Sponsor Dedicated

IQVIA

Paris, France
On-site monitoring experience
Good clinical practice knowledge
Site management skills
The role involves performing monitoring and site management work to ensure compliance with study protocols and regulations

Job Summary

  • The role involves performing monitoring and site management work to ensure compliance with study protocols and regulations.
  • You will collaborate with sites to enhance subject recruitment and manage ongoing project expectations.
  • The position requires maintaining documentation and tracking study progress to ensure quality and integrity.

Matching Summary

The role involves performing monitoring and site management work to ensure compliance with study protocols and regulations.

Skills & Requirements

Must-have

  • On-site monitoring experience
  • Good Clinical Practice knowledge
  • Site management skills

Nice-to-have

  • Organizational skills
  • Problem-solving abilities
  • Effective communication skills

Key Requirements

  • 2 years of monitoring experience
  • Degree in scientific discipline preferred
  • Proficiency in Microsoft Office

Work Rights

Not specified

Tailored Resume

Cover Letter