Clinical Research Assistant

Summary

The Clinical Research Assistant supports the planning, execution, and documentation of clinical studies, working under the guidance of the Principal Investigator and Clinical Research Coordinator to ensure studies run smoothly and comply with protocols and regulations.

Key Responsibilities

• Assist with participant recruitment, screening, and scheduling
• Collect, enter, and verify study data accurately in case report forms (CRFs) or electronic data capture systems
• Maintain study files, regulatory documents, and investigator site files
• Support informed consent processes and ensure documentation is complete
• Help prepare samples, process specimens, and coordinate lab logistics
• Report adverse events and protocol deviations to the study team
• Ensure compliance with GCP, ICH guidelines, and institutional/ethics committee requirements
• Assist with preparing for audits, monitoring visits, and ethics submissions

Qualifications

• Bachelors degree in life sciences, pharmacy, nursing, or a related field
• 0–2 years of experience in clinical research (freshers may be considered)
• Knowledge of GCP and clinical trial processes
• Strong attention to detail, organization, and communication skills
• Proficiency in MS Office and basic data entry tools

Preferred

• GCP certification
• Prior exposure to a hospital or CRO setting