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.
Key responsibilities include supporting clinical supply management, ensuring timely maintenance of tracking tools, and assisting with submission packages to IRB/ERC and Health Authorities.
The position requires acting as a process Subject Matter Expert (SME), making recommendations for continuous improvement, and mentoring junior CTCs.
Matching Summary
This role is responsible for comprehensive trial and site administration, including preparing, collating, distributing, and archiving clinical documents.