Perform on-site monitoring visits as well as site identification, feasibility and selection as required
Responsible for evaluating, initiating, monitoring and closing out clinical study sites
Ensure clinical projects are conducted, recorded, and reported in accordance with the project protocol
Comply with Good Clinical Practice (GCP), Company SOPs and all applicable regulatory requirements
Provide ongoing updates and support to project management
Master’s Degree certificate
4 months of experience or a Master's in clinical research before obtaining the certification (the Master in the 36 months prior to get the certification)
Certificate of 40 hours of theoretical training
20 days of co-monitoring visits to CRA already certified (of which 50% at the centres)
In possession of CRA Certification according to Ministerial Decree 15/11/2011
Fluent in English and Italian
If you’re interested in this role, please get in touch and I will be happy to discuss this in further detail: +44 1273 952187.
Salary: On application
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