Education
Work Experience
Technical Knowledge, Skills, and Abilities
The Clinical Research Data Coordinator I manages the data for assigned research studies. This will include, designing forms for data collection, clinical data abstraction, reconciling data, maintaining record systems, and producing project reports for studies. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the data coordinator plays a critical role in the study by reviewing, extracting, cleaning, and auditing data from various source documents so that the appropriate data can be shared.
Essential Functions
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