(senior) Clinical Research Associate - Sponsor Dedicated - Türkiye

IQVIA UK

Türkiye
Site selection and monitoring
Ich and gcp guidelines
Regulatory submission tracking
Perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan

Job Summary

  • Perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan.
  • Evaluate the quality and integrity of site practices in accordance with regulatory requirements like GCP and ICH guidelines.
  • IQVIA offers resources for career growth, supportive leaders, programs to build therapeutic knowledge, and a better work-life balance.

Matching Summary

Perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan.

Skills & Requirements

Must-have

  • site selection and monitoring
  • ICH and GCP guidelines
  • regulatory submission tracking
  • subject recruitment planning

Nice-to-have

  • flexible work schedules
  • career growth resources
  • therapeutic knowledge building

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter