Clinical Research Associate

LLRI - Learning Labb Research Institute; Bengaluru; On-site; INR 300,000 - 450,000; Full time

Job summary

LLRI - Learning Labb Research Institute in Bengaluru seeks an entry-level Clinical Research Associate to monitor trial sites, verify data quality and ensure GCP compliance and patient safety across assigned studies. Fresher or 0-1 year of experience is welcome; on-the-job training will be provided.

Candidates with B.Pharm/BSc Life Sciences and a willingness to learn will fit well. You will support site visits, data verification, TMF maintenance and coordination with investigators and sponsor

Qualifications

• Freshers / 0-1 year experience; willing to learn and on-the-job training will be provided.
• Educational background in clinical research or life sciences is preferred.
• Attention to detail and good documentation discipline are desirable.

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 study protocol.
• Track patient enrolment and informed consent process.
• 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.

Skills

Clinical Research

GCP Compliance

Patient Safety

Documentation

Education

B.Pharm/M.Pharm

BSc/MSc Life Sciences

BDS

BPT

PG Diploma in Clinical Research

Tools

MS Office

Word

Excel

PowerPoint

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