Role 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■ Valuable written and verbal communication skills

n■ Attention to detail and documentation discipline

n■ Willingness to learn and work in a regulated, compliance-driven environment

n■ Willingness to travel for site visits

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