Clinical Research Associate

Role OverviewAn entry-level Clinical Research Associate (CRA) to monitor clinical trial sites, verify data quality andensure 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 filesKey Skills & Keywords (ATS Optimised)Must-Have Keywords:Clinical Research | Clinical Trials | GCP Compliance | Patient Safety | Clinical Trial ManagementAdditional / Good-to-Have Keywords:CRO | Data Quality | Pharmaceutical | Life Sciences | Research | HealthcareEducational QualificationB.Pharm/M.Pharm, B.Sc/M.Sc Life Sciences, BDS, BPT, or PG Diploma in Clinical Research.Experience RequiredFresher / 0-1 year. Freshers with the right educational background and a willingness to learn arestrongly 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