Experienced Clinical Research Associate, Iqvia Biotech - Home Based, Italy

IQVIA

Milan, Italy
Perform site monitoring visits
Administer protocol and study training
Evaluate study site quality
Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor

Job Summary

  • Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor.
  • Evaluate the quality and integrity of study site practices related to protocol conduct and adherence to regulations, escalating issues as appropriate.
  • Manage study progress by tracking submissions, recruitment, CRF completion, and data query resolution, ensuring TMF and ISF are maintained.

Matching Summary

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

Skills & Requirements

Must-have

  • Perform site monitoring visits
  • Administer protocol and study training
  • Evaluate study site quality
  • Manage study progress and documentation
  • Ensure TMF and ISF maintenance

Nice-to-have

  • Adapt and drive subject recruitment
  • Collaborate with study team members
  • Support project execution
  • Establish effective working relationships

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter