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Research Documentation Specialist

1 week ago

Singapore This is an IT support group Full time
Job Summary
We are seeking an experienced Clinical Trials Assistant to join our team. In this role, you will be responsible for assisting CRAs and RSU with various tasks related to clinical document management. Your strong organizational skills and attention to detail will ensure the accuracy and timeliness of clinical documentation and reports.

Key Responsibilities
  1. Update and maintain clinical documents and systems to track site compliance and performance.
  2. Collaborate with the clinical team to prepare, handle, distribute, file, and archive clinical documentation and reports.
  3. Participate in reviewing study files for completeness.
  4. Coordinate the preparation, handling, and distribution of Clinical Trial Supplies.
  5. Manage CRFs, queries, and clinical data flow.
  6. Act as a central point of contact for designated project communications and correspondence.