Clinical Research Associate
Support trials that bring treatments to patients
Meridian Life Sciences · Mumbai
Job Description
Meridian Life Sciences is hiring a Clinical Research Associate to monitor clinical trial sites for GCP compliance and data quality across multiple ongoing studies. You will conduct regular site visits, building working relationships with investigators and site coordinators so issues get raised early rather than discovered during an audit, and you will review case report forms line by line for accuracy and completeness, catching discrepancies that could otherwise compromise trial data integrity. You will coordinate with investigators and third-party vendors on trial logistics, supply shipments, lab kit timing, equipment calibration, where a single missed detail can delay a site's enrollment for weeks. You will maintain regulatory documentation to audit-ready standards at all times, since regulatory inspections can happen with little notice, and you will track site performance against enrollment targets, escalating underperforming sites early enough that corrective action is still possible. You will also identify and escalate protocol deviations promptly and accurately, understanding that how a deviation is documented matters as much as the deviation itself for trial integrity. Prior CRA experience is preferred, though a strong clinical trial coordination background from a site or sponsor side will also be seriously considered.
Designation: Clinical Research Associate
Location: Mumbai
Industry: Pharmaceuticals / Life Sciences