To independently perform and coordinate clinical data management activities for assigned clinical studies, ensuring accurate, complete, consistent, and GCP/regulatory‑compliant clinical trial data.
- Accountable for executing assigned clinical data management activities in accordance with study requirements, timelines, SOPs, and regulatory guidelines.
- Accountable for performing data review, validation, and cleaning activities to ensure data accuracy, completeness, and consistency.
- Accountable for raising, tracking, and facilitating timely resolution of data queries with investigative sites and internal stakeholders.
- Accountable for monitoring CRF/eCRF completion, query status, and data discrepancies to support study milestones.
- Accountable for supporting CRF/eCRF review, database testing, and User Acceptance Testing (UAT) activities as assigned.
- Bachelor's or Master's degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, Health Sciences, or a related discipline.
