Clinical Research Associate - Iqvia Biotech (homebased In Paris)

IQVIA UK

Paris, France
Site monitoring visits
Gcp and ich guidelines
Subject recruitment plan
At IQVIA Biotech, we partner with visionary biotech companies to transform innovation into patent impact

Job Summary

  • At IQVIA Biotech, we partner with visionary biotech companies to transform innovation into patent impact.
  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.

Matching Summary

At IQVIA Biotech, we partner with visionary biotech companies to transform innovation into patent impact.

Skills & Requirements

Must-have

  • site monitoring visits
  • GCP and ICH guidelines
  • subject recruitment plan
  • protocol and study training
  • quality and integrity evaluation
  • Trial Master File (TMF)

Nice-to-have

  • deep therapeutic expertise
  • biotech tailored model
  • accelerate clinical development
  • effective time management
  • problem-solving skills

Key Requirements

  • Minimum 1 year monitoring experience
  • Life Science, Nursing, Pharmacy or medical degree
  • Basic knowledge of GCP and ICH
  • Proficiency in Microsoft Office Suite
  • Good command of English language

Work Rights

Not specified

Tailored Resume

Cover Letter