Clinical Research Associate

IQVIA

Istanbul, Turkey
Gcp and ich guidelines adherence
High-quality monitoring activities
Site management and communication
The role involves performing high-quality monitoring and site management activities to ensure clinical trials are executed successfully

Job Summary

  • The role involves performing high-quality monitoring and site management activities to ensure clinical trials are executed successfully.
  • Responsibilities include conducting site visits, developing recruitment plans, providing training, and ensuring regulatory compliance.
  • IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence.

Matching Summary

The role involves performing high-quality monitoring and site management activities to ensure clinical trials are executed successfully.

Skills & Requirements

Must-have

  • GCP and ICH guidelines adherence
  • High-quality monitoring activities
  • Site management and communication
  • Protocol compliance assessment
  • Clinical research processes knowledge

Nice-to-have

  • Strong cross-functional collaboration
  • Excellent organizational skills
  • 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