General role description

Clinical Research Associates (CRAs) are responsible for monitoring clinical trials that test new treatments. They help ensure that trials follow strict guidelines and are conducted safely and ethically. CRAs check that trial data is accurate and support the clinical teams by answering questions on the trial protocol, providing training or clarification on documentation or data and data entry, and flagging issues early to keep the trial on track. CRAs conduct monitoring visits at study sites, which are often in hospitals, clinical, and laboratory settings. In more recent times, hybrid models have been introduced allowing effective oversight through virtual monitoring tools while conducting needed on-site visits.

Key responsibilities

• Monitor clinical trial sites and ensure they follow protocols
• Review trial data for accuracy and completeness
• Support site setup and assist in staff training
• Maintain documentation and prepare reports
• Ensure trials follow Good Clinical Practice (GCP) and regulatory standards