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 progress

Eligibility 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