Clinical Research Coordinator

Role & responsibilities

A Clinical Research Coordinator (CRC) to manage day-to-day clinical trial activities at the site level,

working closely with investigators, patients and sponsors.

Key Responsibilities

Coordinate patient recruitment, screening and the informed consent process at site

Schedule and manage patient visits as per the study protocol

Maintain accurate Case Report Forms (CRFs) and source documents

Liaise with CRAs/monitors, investigators and sponsor/CRO teams

Ensure protocol and GCP compliance at the site

Track and report adverse events to support patient safety

Manage investigational product accountability and site regulatory files

Preferred candidate profile

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

Comfortable interacting directly with patients