Experienced Clinical Research Associate Sponsor-dedicated

IQVIA UK

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.
  • 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
  • Subject recruitment plan
  • Protocol and study training
  • Quality and integrity evaluation
  • Trial Master File maintenance
  • Site documentation and reporting

Nice-to-have

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

Key Requirements

  • 2 years on-site monitoring experience
  • GCP and ICH guidelines knowledge
  • Proficiency in Microsoft Office Suite
  • Fluent in Greek and English

Work Rights

Not specified

Tailored Resume

Cover Letter