Location
são paulo, são paulo, Brazil
Posted
July 13, 2026
Job Description
Overview
Under the oversight of the line‑manager, this role is responsible for comprehensive trial and site administration, including preparing, collating, distributing, and archiving clinical documents. The role supports clinical supply and non‑clinical supply management, maintains tracking and reporting tools, and ensures site readiness and financial compliance.
Responsibilities
- Trial and site administration
- Track essential documents
- Ensure collation and distribution of study tools and documents
- Update clinical trial databases (CTMS) and trackers
- Document management
- Prepare documents and correspondence
- Collate, distribute/ship, and archive clinical documents (e.g., eTMF)
- Assist with eTMF reconciliation
- Execute eTMF Quality Control Plan
- Prepare investigator trial file binders
- Obtain translations of documents
- Budgeting, agreement and...