Clinical Research Coordinator
Support study documentation, compliance management, and data entry tasks.
Key Responsibilities:
* Administrative duties including general office work
* Manage documentation in accordance with regulatory requirements
* Track training and certification records
* Coordinate protocol training activities
* Enter and assist with clinical data entry
Requirements:
* Certificate III/IV in Administration or equivalent experience
* Background in health, research, or administration
* Strong attention to detail and organizational skills
* Familiarity with GCP principles