Overview
On Site
Full Time
Skills
FOCUS
Microsoft Excel
Microsoft PowerPoint
Microsoft Outlook
ServiceNow
Reporting
Pharmaceutics
Computerized System Validation
Veeva
Writing
Test Scripts
Clinical Trial Management System
Job Details
Roles & Responsibilities:
- Right now, the CSV team is focused on UATs, periodic review, test scripts and change controls for their Medidata CTMS and IT ServiceNow Infrastructure projects.
- The focus is to have CSV support the ongoing CTMS. The client is currently bringing a new CTMS in house and just implemented ServiceNow in the last couple of months.
- The team consists of three employees in the CSV department. This group works closely with the IT Business Relationships team and will interact daily with two team members (AD of IT Business Relationships and Head of IT Business Relationships)
- This CSV team will be supporting the clinical operations and clinical system teams with validating the new CTMS as the implementation progresses.
- This CSV team will also support Veeva Quality Docs
- In total there are about 14 projects across three CSV resources that need to be supported.
- The client is looking for a resource to cover UATs, periodic review, and provide a validation summary prior to roll out of the new systems.
- CTMS Medidata
- SharePoint
- Microsoft Office - Excel, Word, Power Point, Outlook
- This consultant will provide/develop UATs, periodic review, and test scripts for the CTMS Medidata
- Validate Veeva Quality Docs
- This consultant will develop change controls specifically for ServiceNow.
- They will report their findings to the Associate Director of IT CSV and Associate Director of IT Business Relationships in support of the IT and clinical departments.
- Previous experience as a CSV consultant at a pharmaceutical company
- Prior experience working on CSV for a CTMS
- Veeva and Medidata (highly preferred)
- Experience validating Veeva Quality Docs
- Previous experience developing UATs
- Prior experience writing test scripts for a CTMS
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