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Clinical Data Manager II
Ref No.: 18-29622
Location: Raritan, New Jersey
Clinical Data Manager II is responsible for CTMS and Grants Management study build, maintenance, and support activities. This position may also be responsible for support of other applications supported by the Clinical Trial Management Solutions group.

Job Description:
Work with Study Teams and partners during study build process to create/maintain the following in CTMS: Study, Country, Site, Contacts, and Institution records
Create and set up templates such as Health Authority, IRB/IEC, Financial Disclosure, Subject Visit, Visit/Trip Report, etc.
Update system dropdown values
Create/Update assignments, configurations, properties, attributes, triggers, and parameters in the system.
User administration
Import/Export templates
Add Payees and study triggers
Visit Schedules
Subject deviations/central findings
Any other general study build activities
Troubleshoot integration errors between CTMS and other applications

Provide Study build activities for Grants Manager
Create study
Upload templates
Create/Add sites
User administration (send invitations)
Any other general study build activities

Assist with UAT activities (draft test scripts, execute test scripts, etc.)
Provide general business support for CTMS and Grants Manager applications
Create/Generate reports
Run SQL queries
Support Ticket generation/creation and maintenance (tracking of issues/requests)
Create/Update reference and training materials/documentation

Education Requirements:
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
1-3 years of professional experience.