Clinical Research Associate

Role Overview An entry-level Clinical Research Associate (CRA) to monitor clinical trial sites, verify data quality and ensure GCP compliance and patient safety across assigned studies.

Key Responsibilities Support and conduct site visits for study initiation, monitoring and close-out Verify source documents against Case Report Forms (CRFs) for data accuracy Ensure clinical trials are conducted as per GCP, ICH guidelines and study protocol Track patient enrolment, informed consent process and protocol adherence Coordinate with investigators, CRO and sponsor teams on trial timelines Support adverse event reporting and patient safety documentation Maintain Trial Master File (TMF) documentation and site files Key Skills & Keywords (ATS Optimised) Must-Have Keywords: Clinical Research | Clinical Trials | GCP Compliance | Patient Safety | Clinical Trial Management Additional / Good-to-Have Keywords: CRO | Data Quality | Pharmaceutical | Life Sciences | Research | Healthcare Educational Qualification B.Pharm/M.Pharm, B.Sc/M.Sc Life Sciences, BDS, BPT, or PG Diploma in Clinical Research.

Experience Required Fresher / 0-1 year. Freshers with the right educational background and a willingness to learn are strongly encouraged to apply. On-the-job training will be provided. Good to Have Basic knowledge of MS Office (Word, Excel, PowerPoint) Good written and verbal communication skills Attention to detail and documentation discipline Willingness to learn and work in a regulated, compliance-driven environment Willingness to travel for site visits .