Job Summary
A company is looking for a Clinical Research Associate (CRA I, II, Sr).
Key Responsibilities
- Conduct site qualifications, initiations, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process
- Support sponsors in the development of oncology therapies during phase I-III studies
Required Qualifications
- Bachelor's degree in a biological or science-related field or equivalent experience
- Prior experience as a Clinical Research Associate managing clinical trial sites
- Experience in monitoring early phase oncology studies is preferred
- The number of years and type of monitoring experience will determine CRA level
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