Job Description
Responsibilities:
Lead CDM activities for assigned clinical studies, ensuring data quality and compliance with study timelines.
Design and/or support the design of clinical databases in alignment with study protocols and requirements, including creation of edit checks and dynamic functionalities.
Conduct User Acceptance Testing (UAT) to validate clinical database functionality and accuracy.
Author, review, and approve study-specific CDM documentation such as Data Management Plans (DMPs), Case Report Form Completion Guidelines (CCGs), Data Transfer Agreements (DTAs), and EDC specifications.
Support data cleaning and validation activities to ensure completeness and accuracy of study data.
Monitor study progress to ensure milestones are met and deliverables are achieved on schedule.
Oversee and manage CDM vendors to ensure high-quality deliverables and adherence to project timelines.
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