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

IQVIA UK

Italy
Good clinical practice (gcp) adherence
International conference on harmonization guidelines
Site initiation and close-out visits
The role involves performing site monitoring visits to ensure studies are conducted according to the protocol and regulatory guidelines

Job Summary

  • The role involves performing site monitoring visits to ensure studies are conducted according to the protocol and regulatory guidelines.
  • Candidates must manage subject recruitment plans and maintain accurate documentation in the Trial Master File and Investigator's Site File.
  • IQVIA is a leading global provider committed to integrity and accelerating the development of innovative medical treatments.

Matching Summary

The role involves performing site monitoring visits to ensure studies are conducted according to the protocol and regulatory guidelines.

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP) adherence
  • International Conference on Harmonization guidelines
  • Site initiation and close-out visits
  • Trial Master File maintenance
  • Subject recruitment plan management

Nice-to-have

  • Strong problem-solving skills
  • Effective client relationship building
  • Flexibility to travel within Italy
  • Experience with financial management of sites

Key Requirements

  • Bachelor's or Master's degree in scientific discipline or health care
  • CRA Certification as required by Ministerial Decree dated 15.11.2011
  • Driver's license class B
  • Excellent command of English language
  • Experience in Pharma Industry or Clinical Trials environment

Work Rights

Not specified

Tailored Resume

Cover Letter