Experienced Clinical Research Associate, Fsp Belgium

IQVIA UK

Zaventem, Belgium
Site selection and initiation
Monitoring and close-out visits
Subject recruitment planning
Perform site selection, initiation, monitoring, and close-out visits to ensure quality and integrity of site practices

Job Summary

  • Perform site selection, initiation, monitoring, and close-out visits to ensure quality and integrity of site practices.
  • Manage progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions.
  • IQVIA offers resources for career growth, supportive leaders, programs to build therapeutic knowledge, and an excellent working environment with attractive benefits.

Matching Summary

Perform site selection, initiation, monitoring, and close-out visits to ensure quality and integrity of site practices.

Skills & Requirements

Must-have

  • site selection and initiation
  • monitoring and close-out visits
  • subject recruitment planning
  • quality and integrity evaluation
  • progress tracking and data query resolution
  • collaboration with site experts

Nice-to-have

  • career growth resources
  • supportive leadership
  • flexible work schedules
  • therapeutic knowledge building
  • international company environment

Key Requirements

  • University degree in scientific discipline or health care
  • Experience in Pharma Industry and/or Clinical Trials
  • Excellent command of Dutch, French and English
  • Belgium based
  • Driver’s license class B

Work Rights

Belgium based

Tailored Resume

Cover Letter