CRA Associate, Italy on 9 month Contract
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. For more information about this opportunity, please contact Adrian Barnard on 020 7318 5261 or email abarnard@primepharmapeople.com
