Document Governance Expert

Vor 5 Tagen


Basel, Basel-Stadt, Schweiz Novartis Farmacéutica Vollzeit

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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