Cra 1

IQVIA UK

Multiple Locations
Site monitoring visits
Good clinical practice (gcp)
International conference on harmonization (ich) guidelines
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.
  • Collaborate and liaise with study team members for project execution support as appropriate.

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
  • Good Clinical Practice (GCP)
  • International Conference on Harmonization (ICH) guidelines
  • subject recruitment tracking
  • clinical trial documentation
  • regulatory submissions tracking

Nice-to-have

  • organizational and problem-solving skills
  • effective communication skills
  • time and financial management
  • collaboration with study teams

Key Requirements

  • Bachelor's Degree in scientific discipline or healthcare preferred
  • completion of CRA training program or prior monitoring experience
  • basic knowledge of clinical research regulatory requirements
  • proficiency in Microsoft Word, Excel and PowerPoint
  • good command of English language

Work Rights

Not specified

Tailored Resume

Cover Letter