Freelance CRA-Clinical Research Associate

Our Medium-Large CRO client is looking for a Freelance CRA or Senior CRA to initiate, monitor and lead a phase II study in Italy. You will be the point of contact for the client in Italy and will work field / home based with an initial 9 month rolling contract.

Typical functions will include but are not be limited too:
• Review and negotiate site regulatory documents and contracts
• Work with Clinical Ops management on site identification project specifics, status and deliverables
• Monitor across site/sites and oversee the progress of the clinical trial
• Complete monitoring reports as well as confirmation and follow-up letters per company Standard operating procedures, provides relevant files and updates for Trial Master File
• Ensure that the trial is conducted, reported and recorded in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and the applicable Regulatory requirements
• Completes on site monitoring (pre-study, initiation, interim and close out visits) in accordance with project specific timelines

Key Requirements:
• Own transport with full driving licence (mileage will be paid)
• MIN 2 years Oncology monitoring experience
• MIN 4 years CRA Experience
• Right to work and live in Italy

The initial study will be for 9 months and be in the area of Oncology so prior Oncology experience of at lease 2 years is a must. This role is only suitable for those working on an hourly rate with a Ltd company or through an umbrella company.

**Oncology, Freelance, CRA, SCRA, field/Home based, Clinical Research Associate, Lead CRA, Principle cra, hourly rate, contractor, Italy, Milan, Rome **