Clinical Research Associate

LLRI - Learning Labb Research Institute; Bengaluru; On-site; INR 300,000 - 550,000; Full time

Job summary

LLRI - Learning Labb Research Institute in Bengaluru, Karnataka, is seeking an entry-level Clinical Research Associate (CRA) to monitor clinical trial sites, ensure GCP compliance and patient safety across assigned studies. The role offers on-the-job training and a foundation in clinical research.

You will assist with site visits, data verification against CRFs, and TMF documentation while learning to coordinate with investigators, CRO and sponsor teams on timelines and study protocols.

Qualifications

• Fresh graduates with the right educational background and a willingness to learn are encouraged to apply.
• On-the-job training will be provided.
• Basic knowledge of MS Office (Word, Excel, PowerPoint).
• Good written and verbal communication skills.

Responsibilities

• Support and conduct site visits for study initiation, monitoring and close-out.
• Verify source documents against CRFs for data accuracy.
• Ensure trials are conducted per GCP, ICH guidelines and protocol.
• Track patient enrolment and informed consent process.
• Coordinate with investigators, CRO and sponsor teams on timelines.
• Support adverse event reporting and patient safety documentation.
• Maintain TMF documentation and site files.

Skills

Clinical Research

Clinical Trials

GCP Compliance

Patient Safety

Clinical Trial Management

Education

B.Pharm

M.Pharm

B.Sc Life Sciences

M.Sc Life Sciences

BDS

BPT

PG Diploma in Clinical Research

Tools

MS Office

Job description

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

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, PowerPoint)
• Good written and verbal communication skills
• Attention to detail and documentation discipline
• Willingness to learn and work in a regulated, compliance-driven environment