Job Description
Data Management:
- Collect and manage clinical trial data from different sources, like forms and electronic systems.
- Make sure the data is accurate, complete, and entered on time.
- Check for errors or mismatches in the data and work with the research team to fix them.
- Help get the data ready for analysis.
Study Documentation:
- Keep study files organized and up-to-date, following all rules and regulations.
- Make sure all required documents, like consent forms and approvals, are current and ready for audits.
- Track important dates and deadlines for the study.
Compliance & Quality Control:
- Review data to make sure it follows study rules and Good Clinical Practice (GCP) guidelines.
- Help prepare for visits and audits from regulatory agencies.
- Ensure the study meets all legal, ethical, and privacy standards.
Collaboration & Communication:
- Work with investigators, coordinators, and other team members to support the study.
- Communicate with outside groups like sponsors, CROs, and regulators to keep data flowing smoothly.
- Create regular updates on how the study is going, including any issues with the data.
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