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, Power Point) ■ Good written and verbal communication skills ■ Attention to detail and documentation discipline ■ Willingness to learn and work in a regulated, compliance-driven setting ■ Willingness to travel for site visits

📌 Clinical Research Associate (Karnataka)
🏢 LLRI - Learning Labb Research Institute
📍 Karnataka