Clinical Research Associate

Job Description

• Protocol Review: Should have appropriate scientific background and the ability to thoroughly review and understand the study protocol, which outlines the objectives, design, methodology, and conduct of the clinical trial.

• Site Selection: Conduct the selection of appropriate clinical trial sites and investigators based on their qualifications and ability to conduct the study.

• Site Initiation: Conduct site initiation visits to train investigators and site staff on the protocol, regulatory requirements, and data collection procedures.

• Monitoring: Conduct monitoring visits and carry out all required activities as outlined in the monitoring plan.

• Data Collection and Management: Oversee site data collection and source documentation activities to ensure clinical trial data are accurate, complete, and ...