Clinical Research Associate

Role Overview

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

Key Skills & Keywords (ATS Optimised)

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

■ Willingness to travel for site visits