Position Overview
Responsibilities:
Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting.
Develop and manage data management timelines for multiple projects, ensuring all milestones are met according to project plans.
Design, build, and oversee the implementation and management of clinical trial databases using Electronic Data Capture (EDC) systems (, Medidata, Medrio, or similar).
Develop and oversee maintenance all data management documentation for all clinical studies.
Ensure clinical data is captured accurately and efficiently, incorporating appropriate data validation checks and edit checks.
Oversee data validation processes, including data cleaning, discrepancy management, and query resolution.
Ensure data accuracy, completeness, and compliance with regulatory requirements (, FDA, EMA) and industry standards (CDISC, SDTM, W...