Experienced Clinical Research Associate, Fsp Belgium

IQVIA Inc

Belgium
Site selection and monitoring
Subject recruitment planning
Quality and integrity evaluation
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 and manage progress by tracking submissions, recruitment, and data query resolutions.
  • IQVIA offers resources for career growth, supportive leaders, programs to build therapeutic knowledge, and an excellent working environment in a stable, international company.

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
  • Subject recruitment planning
  • Quality and integrity evaluation
  • Regulatory submission tracking
  • Collaboration with site experts

Nice-to-have

  • Career growth resources
  • Supportive leadership
  • 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

Not specified

Tailored Resume

Cover Letter