Job DescriptionRole Overview
NAn entry-level Clinical Research Associate (CRA) to monitor clinical trial sites, verify data quality and
Nensure GCP compliance andpatient safety across assigned studies.
NKey Responsibilities
n■ Support and conduct site visits for study initiation, monitoring and close-out
N■ Verify source documentsagainst 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-HaveKeywords:
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 verbalcommunication skills
N■ Attention to detail anddocumentation discipline
N■ Willingness to learn and work in a regulated, compliance-driven workplace
N■ Willingness to travel for site visits

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