Data Manager for Clinical Trials

Track database setup, testing, maintenance, and data entry while designing eCRFs, data management plans, and validation plans. Review study documents to develop project-specific guidelines and instructions. Ensure data entry, follow-up, and validation, including manual CRF review and SAE reconciliation. Code medical data and track metrics leading to database lock. Coordinate CRF processing, dispatch, and archiving, and maintain working files. Perform database QC checks, prepare for audits, and train site staff on CRF completion and data management topics. Based in Brazil, this role requires a College/University degree with demonstrated clinical data management experience and proficiency in Clinical Data Management systems.