Experienced Cra, Sponsor Dedicated - Italy

IQVIA UK

Italy
Not specified (assumed to be hybrid or onsite due to the nature of cra work)
Perform site monitoring visits
Ensure gcp and ich guideline adherence
Manage subject recruitment plans
IQVIA UK is seeking an experienced Clinical Research Associate (CRA) for a sponsor-dedicated position in Italy. The role involves site monitoring and management to ensure compliance with protocols, regulations, and sponsor requirements

Job Summary

  • The role involves performing site monitoring visits to ensure studies are conducted according to the protocol and regulations.
  • Candidates must manage subject recruitment plans and maintain accurate documentation in the Trial Master File.
  • IQVIA is a leading global provider of clinical research services dedicated to accelerating medical treatment development.

Matching Summary

Match Score: 85

IQVIA UK is seeking an experienced Clinical Research Associate (CRA) for a sponsor-dedicated position in Italy. The role involves site monitoring and management to ensure compliance with protocols, regulations, and sponsor requirements.

Skills & Requirements

Must-have

  • Perform site monitoring visits
  • Ensure GCP and ICH guideline adherence
  • Manage subject recruitment plans
  • Maintain Trial Master File documentation
  • Generate visit reports and follow-up letters

Nice-to-have

  • Strong problem-solving skills
  • Effective time management abilities
  • Experience with financial management of sites

Key Requirements

  • Bachelor's or Master's degree in scientific discipline
  • At least 3 years of on-site monitoring experience
  • CRA Certification per Ministerial Decree dated 15.11.2011
  • Proficiency in Microsoft Office and mobile devices

Work Rights

Not specified

Tailored Resume

Cover Letter