Job Summary
The Clinical Research Associate (CRA) plays a crucial role in the management and oversight of clinical trials. This position requires ensuring compliance with regulatory standards and the integrity of the data collected during these trials. The CRA acts as a liaison between the sponsor and the clinical sites, facilitating effective communication and collaboration.
Responsibilities
- Monitor clinical trial sites to ensure compliance with study protocols, regulations, and quality standards.
- Conduct regular site visits to review and verify accuracy of data collected and address any issues.
- Maintain thorough documentation and reports regarding site activities and any deviations from protocols.
- Assist in the training of site staff on study protocols and regulatory requirements.
- Collaborate with cross-functional teams to ensure timely and successful trial execution.
Qualifications
- A degree in life sciences, nursing, or a related field is preferred.
- Previous experience in clinical research or monitoring is advantageous.
- Strong understanding of Good Clinical Practice (GCP) and regulatory guidelines.
- Excellent organizational and communication skills, with attention to detail.
- Ability to work independently as well as part of a team.
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