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).

 

Responsibilities:

  • 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

Requirements:

  • 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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