Experienced Clinical Research Associate Sponsor-dedicated

IQVIA

Athens, Greece
Site monitoring visits
Subject recruitment plan
Protocol and study training
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.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

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
  • Subject recruitment plan
  • Protocol and study training
  • Quality and integrity evaluation
  • Trial Master File (TMF) documentation
  • Investigator's Site File (ISF) maintenance

Nice-to-have

  • Effective time management
  • Problem-solving skills
  • Client relationship management

Key Requirements

  • At least 2 years of on-site monitoring experience
  • Good Clinical Practice (GCP)
  • ICH guidelines
  • Proficiency in Microsoft Word, Excel, PowerPoint
  • Written and verbal communication skills in Greek and English

Work Rights

Not specified

Tailored Resume

Cover Letter