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

Qualifications

• B.Pharm/M.Pharm, B.Sc/M.Sc Life Sciences, BDS, BPT, or PG Diploma in Clinical Research
• 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

Key Skills & Keywords

• Clinical Research
• Clinical Trials
• GCP Compliance
• Patient Safety
• Clinical Trial Management
• CRO
• Data Quality
• Pharmaceutical
• Life Sciences
• Research
• Healthcare