Clinical Research Associate

IQVIA UK

Istanbul, Turkey
Gcp/ich guidelines compliance
Site selection and initiation
Subject recruitment planning
Support the successful execution of clinical trials by performing high-quality monitoring and site management activities

Job Summary

  • Support the successful execution of clinical trials by performing high-quality monitoring and site management activities.
  • Ensure that study sites operate in compliance with protocols, GCP/ICH guidelines, regulatory requirements, and sponsor expectations.
  • Collaborate with cross-functional study team members to support operational excellence.

Matching Summary

Support the successful execution of clinical trials by performing high-quality monitoring and site management activities.

Skills & Requirements

Must-have

  • GCP/ICH guidelines compliance
  • Site selection and initiation
  • Subject recruitment planning
  • Essential document maintenance
  • Monitoring visit reporting

Nice-to-have

  • Strong communication and collaboration
  • Problem-solving abilities
  • Building strong working relationships

Key Requirements

  • Minimum 1 year on-site monitoring experience
  • Bachelor's degree in scientific/healthcare discipline
  • Proficiency in Microsoft Office Suite
  • Strong English communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter