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QC Submissions Coordinator


  • Tech Observer
  • 12/06/18
  • East Hanover, NJ
  • 07936
  • Competitive / Yearly
  • Contractor
W2 contract with direct pharma client based in East Hanover, NJ - New Jersey

Must have: 2+ years' clinical document management experience along with documentum/ sharepoint, & document qc

Duties:
This role will provide operational support to the Oncology QC Submission Manager, Submission Managers and Writers as well as Clinical Submission Teams for submission document QC PROCESS.
The incumbent will support vendor oversight and quality activities including: KPI monitoring, metrics collection and reporting as well as adherence to Oncology Submission Management and NVS Guidelines, SOPs and WPs and have understanding of the QC process.
The QC Coordinator must have practical experience with document management system(s) (preferably Documentum-based) as well as SharePoint and be able to navigate effectively through other web-based and email processes.
The incumbent will also assist in creation of presentation materials using MS Office programs (Word, Excel, PowerPoint).

Skills:
A minimum of 2 years (3-5 preferred) experience in the pharmaceutical industry.
Clinical document management, document QC, and other administrative skills.

Education:
A Bachelor's degree (science or healthcare-related preferred)

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