Experienced Cra, Sponsor Dedicated - Italy

IQVIA UK

Italy
Perform site monitoring visits
Manage study progress
Ensure site compliance with regulations
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements

Job Summary

  • Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Skills & Requirements

Must-have

  • Perform site monitoring visits
  • Manage study progress
  • Ensure site compliance with regulations
  • Maintain Investigator's Site File
  • Create study documentation

Nice-to-have

  • Drive subject recruitment plan
  • Collaborate with study team members
  • Effective time and financial management

Key Requirements

  • 3 years on-site monitoring experience
  • CRA Certification according to Ministerial Decree dated 15.11.2011
  • Good knowledge of GCP and ICH guidelines
  • Bachelor's and Master's Degree in scientific discipline or health care

Work Rights

Not specified

Tailored Resume

Cover Letter