This role is responsible for comprehensive trial and site administration, including preparing, collating, distributing, and archiving clinical documents
Job Summary
This role is responsible for comprehensive trial and site administration, including preparing, collating, distributing, and archiving clinical documents.
The position involves supporting clinical and non-clinical supply management, ensuring timely maintenance of tracking and reporting tools, and assisting with submission packages to IRB/ERC and Health Authorities.
The role requires collaboration with finance/budgeting representatives to manage CTRAs and payments, acting as a process Subject Matter Expert (SME), and mentoring junior CTCs.
Matching Summary
This role is responsible for comprehensive trial and site administration, including preparing, collating, distributing, and archiving clinical documents.