Clinical Research Associate

CRA Italy

Join our global team as a Clinical Research Associate (CRA).

Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of studies and clinical trials at investigational sites.

Position is in Italy (home based).



  • Study site monitoring and management (site selection, initiation, monitoring and close-out visits)
  • Perform feasibilities and support start-up phase
  • Create and maintain required study documentation (site management, monitoring, etc.)
  • Ensure that clinical trials are conducted according to requirements (protocol, ICH-GCP, etc.)
  • Administer protocol and related study training to assigned sites
  • Assist in regulatory document review and submission to regulatory authorities
  • Prepare clinical trial documents and store, archive correspondence
  • Negotiate study budgets with potential investigators/sites, assit in agreements


  • University degree in Life Science field
  • Fluent English language
  • At least 2 years’ experience as CRA (independent monitoring)
  • In depth therapeutic and protocol knowledge
  • Deep knowledge of local regulations and clinical research regulatory requirements (GCP and ICH)
  • Excellent skills in MS Office, EDC and other clinical trial related systems and platforms
  • Attention to detail and time-management skills

Benefits of being a part of our team:

  • Professional growth and career opportunities
  • Supportive work environment
  • Additional benefits (bonus system, additional health insurance and etc.)
  • International team
Job Category: Clinical Research
Job Type: Full Time
Job Location: Italy
Job Specification: R2

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