What does a remote clinical research associate (CRA) do?

Remote Clinical Research Associates (CRAs) play a vital role in the pharmaceutical and healthcare industries by monitoring and managing clinical trials conducted at multiple sites. Their responsibilities include verifying that trials comply with regulatory requirements, ensuring participant safety, and accurately documenting trial data. CRAs conduct site visits or remote assessments to review study protocols, monitor data collection processes, and resolve any issues that may impact the validity or integrity of the trial results. They collaborate closely with investigators, sponsors, and regulatory authorities to ensure trials are conducted ethically and in accordance with established protocols.