Clinical Research Associate - Sponsor Dedicated

IQVIA UK

Paris, France
Site monitoring visits
Protocol adherence
Regulatory requirements
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements

Job Summary

  • Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
  • At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.

Matching Summary

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Skills & Requirements

Must-have

  • site monitoring visits
  • protocol adherence
  • regulatory requirements
  • GCP and ICH guidelines
  • subject recruitment plan

Nice-to-have

  • pushing boundaries
  • human science and data science
  • intellectual courage

Key Requirements

  • 2 years on-site monitoring experience
  • High School Diploma or equivalent
  • Good knowledge of regulatory requirements
  • Good command of English language

Work Rights

Not specified

Tailored Resume

Cover Letter