(senior) Clinical Research Associate - Sponsor Dedicated - Türkiye

IQVIA

Türkiye
Site selection and initiation
Monitoring site practices
Tracking regulatory submissions
Perform site selection, initiation, monitoring and close-out visits

Job Summary

  • Perform site selection, initiation, monitoring and close-out visits.
  • Evaluate the quality and integrity of site practices in accordance with regulatory requirements.
  • IQVIA offers resources that promote career growth, flexible work schedules, and programs to help build therapeutic knowledge.

Matching Summary

Perform site selection, initiation, monitoring and close-out visits.

Skills & Requirements

Must-have

  • site selection and initiation
  • monitoring site practices
  • tracking regulatory submissions
  • GCP and ICH guidelines
  • Excellent command of Turkish and English

Nice-to-have

  • career growth resources
  • flexible work schedules
  • therapeutic knowledge building
  • better work-life balance

Key Requirements

  • University degree in scientific discipline
  • At least 2 years on-site monitoring experience
  • Good knowledge of clinical research regulatory requirements
  • Driver’s license class B

Work Rights

Not specified

Tailored Resume

Cover Letter