Document Governance Expert
Vor 5 Tagen
About Clinical Document Management
Clinical document management is critical to the success of our clinical trials. We are seeking a skilled Clinical Document Specialist to join our team.
Responsibilities
- Responsible for timely assessment of quality and completeness of clinical documents for an assigned portfolio of studies.
- Identify and communicate clinical document risks/trends/patterns and work with key stakeholders to define and implement pragmatic remediations.
- Execute vendor oversight plan, monitor service metrics, and identify opportunities for improvement to the operating model. Act as point of escalation for issues.
About This Role
This is a hybrid role and can be based in various offices. The expectation is to be in the office 12 days/month.
You'll have the opportunity to:
Drive implementation of Clinical Document Governance Management initiatives, projects and process improvement activities to enhance clinical document management systems, processes and standards at Novartis.
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