Clinical Research Associate, Sponsor Dedicated - Italy

IQVIA UK

Milan, Italy
Site selection and monitoring
Subject recruitment planning
Quality and integrity evaluation
Performing site selection, initiation, monitoring and close-out visits, and supporting the development of a subject recruitment plan

Job Summary

  • Performing site selection, initiation, monitoring and close-out visits, and supporting the development of a subject recruitment plan.
  • Evaluating the quality and integrity of site practices in accordance with regulatory requirements and managing progress by tracking regulatory submissions, recruitment, and data query resolutions.
  • IQVIA offers resources that promote career growth, supportive leaders, programs to build therapeutic knowledge, and an excellent working environment with a company car, mobile phone, and attractive benefits package.

Matching Summary

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

Skills & Requirements

Must-have

  • site selection and monitoring
  • subject recruitment planning
  • quality and integrity evaluation
  • regulatory submissions tracking
  • case report form completion

Nice-to-have

  • effective working relationships
  • flexible work schedules
  • therapeutic knowledge building
  • international reputable company

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