Experienced Cra - Sweden

IQVIA UK

Stockholm, Sweden
Perform site monitoring visits
Ensure study protocol adherence
Manage study progress tracking
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

  • perform site monitoring visits
  • ensure study protocol adherence
  • manage study progress tracking
  • maintain Trial Master File
  • evaluate site quality and integrity

Nice-to-have

  • adapt subject recruitment plan
  • support project execution
  • establish effective communication

Key Requirements

  • at least 2 years on-site monitoring experience
  • Bachelor's Degree in scientific discipline or health care preferred
  • Good Clinical Practice (GCP) knowledge
  • ICH guidelines knowledge
  • Proficiency in Microsoft Word, Excel and PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter