Clinical Data Manager
On-site · Spring House, Pennsylvania, United States
Job Summary
Clinical Data Manager responsible for end-to-end CTMS study build activities. Lead the creation and maintenance of records for Study, Country, Site, Contacts, and Institution; create templates (Health Authority, IRB/IEC, Financial Disclosure, Subject Visit, Visit/Trip Report, etc.); update dropdown values; configure assignments, properties, attributes, triggers, and parameters; manage user administration and template import/export; add Payees and study triggers; manage Visit Schedules and subject deviations; troubleshoot CTMS integration with other applications; provide study build activities for Grants Manager; create studies, upload templates, and add sites; support UAT and provide general business support for CTMS and Grants Manager; generate reports; run SQL queries; handle support tickets; create/update reference and training materials/documentation.
Required Qualifications
- University/college degree is required; preferred in health, computer science, business, engineering, or information technology
- Preferred prior experience with Medidata CTMS and/or Siebel CTMS or other Clinical Trial Management systems
- Knowledge of the Clinical Trial Management process
- Oracle SQL experience is preferred but not required
- 3 - 5 years of professional experience
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