(senior) Clinical Research Associate (cra)

IQVIA

Multiple Locations
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.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

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
  • ICH guidelines
  • GCP knowledge

Nice-to-have

  • effective time management
  • problem-solving skills
  • team collaboration
  • client relationships

Key Requirements

  • at least 2 years of on-site monitoring experience
  • Bachelor's Degree in scientific discipline or health care preferred
  • Good Clinical Practice (GCP) knowledge
  • ICH guidelines knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter