인재풀 - Cra (home-based/hybrid, 상시모집)

Thermo Fisher Scientific UK

United Kingdom
Risk-based monitoring approach
Data accuracy through sdr, sdv, crf review
Ich gcps, applicable regulations
Our Clinical Operations colleagues provide end-to-end assistance for clinical trials on a global scale

Job Summary

  • Our Clinical Operations colleagues provide end-to-end assistance for clinical trials on a global scale.
  • Monitors investigator sites with a risk-based monitoring approach and ensures data accuracy through SDR, SDV, and CRF review.
  • Our Mission is to enable our customers to make the world healthier, cleaner and safer.

Matching Summary

Our Clinical Operations colleagues provide end-to-end assistance for clinical trials on a global scale.

Skills & Requirements

Must-have

  • risk-based monitoring approach
  • data accuracy through SDR, SDV, CRF review
  • ICH GCPs, applicable regulations
  • clinical trial site initiation
  • trial close out and retrieval

Nice-to-have

  • customer focus through good listening
  • flexibility and adaptability
  • contribute to process improvement
  • collaboration with clients

Key Requirements

  • 2+ years as a clinical research monitor
  • Bachelor's degree or equivalent experience
  • Registered Nursing certification
  • Valid driver's license where applicable

Work Rights

Not specified

Tailored Resume

Cover Letter