Freelance CRA-Clinical Research Associate
- or -
Post a project like this£55/hr(approx. $72/hr)
- Posted:
- Proposals: 0
- Remote
- #39206
- Expired
Description
Experience Level: Expert
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 **
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 **
Adrian B.
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Last project
12 Oct 2024
United Kingdom
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