Job DescriptionRole Overview
nAn entry-level Clinical Research Associate (CRA) to monitor clinical trial sites, verify data quality and
nensure GCP compliance and patient safety across assigned studies.
nKey Responsibilities
n■ Support and conduct site visits for study initiation, monitoring and close-out
n■ Verify source documents against Case Report Forms (CRFs) for data accuracy
n■ Ensure clinical trials are conducted as per GCP, ICH guidelines and study protocol
n■ Track patient enrolment, informed consent process and protocol adherence
n■ Coordinate with investigators, CRO and sponsor teams on trial timelines
n■ Support adverse event reporting and patient safety documentation
n■ Maintain Trial Master File (TMF) documentation and site files
nKey Skills & Keywords (ATS Optimised)
nMust-Have Keywords:
nClinical Research | Clinical Trials | GCP Compliance | Patient Safety | Clinical Trial Management




nAdditional / Good-to-Have Keywords:
nCRO | Data Quality | Pharmaceutical | Life Sciences | Research | Healthcare
nEducational Qualification
nB.Pharm/M.Pharm, B.Sc/M.Sc Life Sciences, BDS, BPT, or PG Diploma in Clinical Research.
nExperience Required
nFresher / 0-1 year. Freshers with the right educational background and a willingness to learn are
nstrongly encouraged to apply. On-the-job training will be provided.
nGood to Have
n■ Basic knowledge of MS Office (Word, Excel, PowerPoint)
n■ Good written and verbal communication skills
n■ Attention to detail and documentation discipline
n■ Willingness to learn and work in a regulated, compliance-driven workplace
n■ Willingness to travel for site visits

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