Job Summary
A company is looking for a Contract CRA.
Key Responsibilities
- Conduct monitoring visits for oncology clinical trials
- Ensure compliance with regulatory requirements and study protocols
- Collaborate with study teams to facilitate project progress
Required Qualifications
- Extensive and recent experience in oncology monitoring
- Strong knowledge of RECIST guidelines and their application
- Ability to start immediately
- Experience with compliance processes in clinical research
- Contract position availability
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