Site Coordinator, Clinical Trials
Airvin Skills · Hyderabad · hybrid · Posted 43d ago
About a minute. You'll make an account on the way through.
About this role
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
Sourced from naukri