- Apply basic clinical research methodologies to meet protocol and regulatory requirements.
- Assist in the development of client deliverables like documentation, operating procedures, and workflows.
- Process, monitor, verify, and track receipt of project documentation.
- Interact with clinical site staff regarding study activities and inquiries.
- Perform general quality checks of documentation.
- Prepare correspondence, meeting minutes, and project reports.
- Provide logistical support for committee and DSMB meetings.
- Update spreadsheets and tracking tools to reflect project status.
- Identify, investigate, and resolve project problems.
- Maintain clinical research files and related documents.
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