Clinical Research Associate, Sponsor Dedicated - Italy

IQVIA Inc

Italy
Site selection and monitoring
Subject recruitment planning
Quality and integrity evaluation
Performing site selection, initiation, monitoring and close-out visits to ensure quality and integrity of site practices

Job Summary

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

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

Skills & Requirements

Must-have

  • site selection and monitoring
  • subject recruitment planning
  • quality and integrity evaluation
  • progress management
  • collaboration with experts

Nice-to-have

  • career growth resources
  • flexible work schedules
  • therapeutic knowledge building
  • excellent working environment

Key Requirements

  • University Bachelor's and Master's Degree
  • CRA Certification
  • Experience in Pharma Industry/Clinical Trials
  • Very good computer skills
  • Excellent command of English
  • Driver’s license class B

Work Rights

Not specified

Tailored Resume

Cover Letter