Site Coordinator, Clinical Trials

Role & responsibilities

A Site Coordinator to manage day-to-day coordination at a clinical trial site, ensuring smooth conduct of

studies as per protocol and GCP guidelines.

Key Responsibilities

Coordinate patient scheduling, screening and follow-up visits at the site

Maintain source documents, CRFs and regulatory site files

Support the informed consent process for study participants

Liaise with CRAs, investigators and sponsor/CRO teams

Track investigational product supply and site inventory

Report adverse events and support patient safety monitoring

Ensure site-level GCP and protocol compliance

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 working directly with patients at the site