Sr. Cra 1 - Single Sponsor Dedicated

IQVIA UK

Reading, United Kingdom
Perform site monitoring visits
Manage study progress and data
Ensure gcp and regulatory adherence
Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor requirements

Job Summary

  • Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor requirements.
  • Evaluate the quality and integrity of study site practices related to protocol conduct and adherence to regulations, escalating quality issues as appropriate.
  • Create and maintain documentation regarding site management, monitoring visit findings, and action plans, collaborating with study team members for project execution support.

Matching Summary

Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor requirements.

Skills & Requirements

Must-have

  • Perform site monitoring visits
  • Manage study progress and data
  • Ensure GCP and regulatory adherence
  • Site document management
  • Effective communication with sites

Nice-to-have

  • Drive and track subject recruitment
  • Support project start-up phase
  • Site financial management

Key Requirements

  • 2 years on-site monitoring experience
  • Knowledge of GCP and ICH guidelines
  • Bachelor's Degree in scientific discipline or health care preferred

Work Rights

Not specified

Tailored Resume

Cover Letter