Clinical research associate (CRA)

The main responsibilities of a CRA include:

• Coordination of clinical trials: he/she plans and organizes the different phases of clinical trials, ensuring that all stages are carried out in accordance with established protocols and current regulations.
  Patient recruitment: The CRA participates in the recruitment of eligible patients for clinical trials, in collaboration with doctors and other members of the research team.
• Data collection and management: he/she is responsible for collecting, verifying and managing patient data, ensuring that all information is accurate and complete.
• Patient monitoring: he/she monitors patients throughout the clinical trial, ensuring their safety and responding to their questions or concerns.
• Regulatory compliance: he/she ensures that the clinical trial complies with local and international regulations, as well as good clinical practices (GCP).
• Communication: he/she serves as a link between the various stakeholders of the clinical trial, including investigators, sponsors, regulatory authorities and patients.
• Reporting and Documentation: he/she prepares and submits necessary reports to regulatory authorities and sponsors, and maintains complete and accurate documentation of the clinical trial.

CRAs play a crucial role in the development of new medical treatments, helping to ensure that clinical trials are conducted ethically, safely and effectively.