Job Detail
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- Job Title: Clinical Trials Data Coordinator
- Department: Office of Clinical Trials
- Full/Part Time: Full
- Req Number: UHS-31119
Position Summary:
?Responsible for extracting protocol specific data from research source documents for 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.
In addition:
Provide monthly metric reports to COE leaders
Maintain up to date clinical trials list for providers
Maintain OCT Website
Maintain internal reports related to projects and quality & safety
Schedule meetings with physicians and sponsor partners
Position Qualification:
Associates degree (A.A.) or equivalent from two-year college or technical school.
Two years related experience; or equivalent combination of education and experience.
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