Using expertise developed from system knowledge, this position will advise on the design and develop and assist in the review of reports from the Clinical Trials Management System (CTMS) Oncore. The position will be responsible for preparing, maintaining, advising and assisting in review and interpretation of data from the CTMS Oncore.
The position will be responsible for the maintenance of the Human Subjects Research Portals. These Redcap based forms require regular review and expert knowledge in maintenance, edits and revisions. Reports from the Redcap system will also be managed by this position.
The position works directly with Director, Clinical Research Administration and requires the ability to write reports using SQL as well as an reasonable understanding of Redcap in order to successfully manage its duties. This position reports directly to the Director, Clinical Research Administration
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