Remote
•
Today
Key Responsibilities Design, build, and maintain clinical trial databases as per study protocol and CRF requirements Develop and review Data Management Plans (DMPs), edit check specifications, and validation rules Oversee data cleaning, discrepancy management, and query resolution Perform interim and final database lock activities Ensure data quality, completeness, and consistency throughout the study lifecycle < data-start="1144" data-end="1174">DTA Vendor Management Act as the primary point of
Easy Apply
Contract, Third Party
Depends on Experience
