Junior Clinical Research Associate’s

Responsibilities:

• 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

Requirements:

• 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