Experienced Clinical Research Associate - Sponsor Dedicated - Türkiye

IQVIA

Türkiye
Site selection and monitoring visits
Subject recruitment plan development
Quality and integrity evaluation
Performing site selection, initiation, monitoring and close-out visits is a key responsibility

Job Summary

  • Performing site selection, initiation, monitoring and close-out visits is a key responsibility.
  • You will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
  • Company car, mobile phone and attractive benefits package are offered.

Matching Summary

Performing site selection, initiation, monitoring and close-out visits is a key responsibility.

Skills & Requirements

Must-have

  • Site selection and monitoring visits
  • Subject recruitment plan development
  • Quality and integrity evaluation
  • Progress tracking and data query resolution
  • Collaboration with site experts and clients
  • Excellent command of Turkish and English

Nice-to-have

  • Gain experience in therapeutic areas
  • Build a meaningful career
  • Support flexible work schedules
  • Build therapeutic knowledge

Key Requirements

  • University degree in scientific discipline or health care
  • At least 6 months on-site monitoring experience
  • Experience in Pharma Industry and/or Clinical Trials
  • Driver’s license class B

Work Rights

Not specified

Tailored Resume

Cover Letter