Clinical Trials Assistant II
Core
Support clinical studies by maintaining accurate documentation, coordinating study activities, and ensuring project compliance.
Role type
Clinical Trials Assistant (CTA II)
Builds
Clinical trial documentation and supply tracking systems
Domain
Clinical research / Life sciences
Deliverable
dashboards & analysis
Required skills
Trial Master File (TMF) management, document preparation and archiving, study file compliance review, clinical trial supply coordination, CRF tracking, data workflow assistance
Preferred skills
Science degree, administrative or healthcare coordination experience, Microsoft Office proficiency
Responsibilities
Maintain and update Trial Master Files (TMF) and study documentation; Support document preparation, filing, tracking, and archiving; Review study files for completeness and compliance; Coordinate clinical trial supplies and tracking records; Assist with CRF tracking, study queries, and data workflows; Act as a key contact for project communications and documentation