Job Detail
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- Job Title: Clinical Trials Data Coordinator
- Department: Office of Clinical Trials
- Full/Part Time: Full
- Req Number: UHS-30768
Position Summary:
Responsible for extracting protocol specific data from research source documents and/or clinical trial Case Report forms. Responsible for entering data into clinical trial sponsors' multiple electronic data capture systems. Resolves queries from sponsors regarding data entered in their eCRF systems. Responsible for managing sponsor monitoring visits and serving as first-line interface with sponsor Clinical Monitors (Auditors). Retrieves, logs and ships biological specimens according to protocol requirements. Maintains accuracy, quality and timeliness of data generated by clinical research records. Responsible for maintaining up to date database of CVs, licenses, CITI training documentation, etc., for all research staff. Assists in developing and preparing documents related to research projects.
Position Qualification:
2 year degree/certificate or equivalent experience
1 year clinical/research experience
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