Experienced Clinical Research Associate, Iqvia Biotech - Home Based, Italy

IQVIA UK

Milan, Italy
Good clinical practice (gcp)
International conference on harmonization (ich)
Site monitoring visits
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 project expectations.
  • The position requires strong organizational skills and the ability to maintain effective communication with study team members.

Matching Summary

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

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP)
  • International Conference on Harmonization (ICH)
  • site monitoring visits

Nice-to-have

  • organizational skills
  • flexibility to travel
  • effective working relationships

Key Requirements

  • Bachelor's Degree in scientific discipline
  • CRA Certification
  • experience in Pharma Industry

Work Rights

Not specified

Tailored Resume

Cover Letter