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.
Skills & Requirements
Must-have
Clinical Trial Management Systems (CTMS)
eTMF management and reconciliation
Clinical supply management
Regulatory submissions support
Budget and payment management
ICH-GCP Knowledge
Nice-to-have
Proactive problem-solving attitude
Growth mindset
Culturally sensitive working relationships
Customer focus
Mentoring junior staff
Key Requirements
Minimum 3 - 5 years in Clinical Research or relevant healthcare experience
Completed job training (office management, administration, finance, health care preferred) or Bachelor’s Degree
Fluent in Local Languages and business proficient in English