Clinical Research Associate

Job Summary:We are looking for a motivated and detail-oriented fresher to join as a Clinical Research Associate (CRA). The candidate will assist in monitoring clinical trials, ensuring compliance with protocols, GCP guidelines, and regulatory requirements.Key Responsibilities: Assist in monitoring clinical trial sites and activities Ensure accurate data collection and documentation Support site initiation, monitoring, and close-out visits Maintain trial master files (TMF) and study records Coordinate with investigators and site staff Ensure compliance with Good Clinical Practice (GCP) guidelines Report deviations, adverse events, and study progressEligibility Criteria: Bachelor's degree in Life Sciences, Pharmacy, Nursing, or related field Strong understanding of clinical research basics (preferred) Good communication and documentation skills Willingness to travel for site visits