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We are a central support function within Research & Development supporting Global Clinical Operations (GCO) colleagues worldwide in preparation/support of clinical trials procedures.
As Clinical Research Scientist (m/f/d) you are a global contact for colleagues within and outside GCO in questions about internal standards/procedures in management of clinical trials. You will also work with our main contact persons from other Teva departments (e.g. Legal, Quality Assurance, Business Conduct Compliance) on a wide range of topics and, if necessary, you will be in contact with external partners.
Your tasks include maintenance and update of GCO vendor portfolio including the independent, reliable vendor maintenance and updating of the GCO SharePoint vendor information page.
You will also support the development of new global processes for GCO and contribute to the harmonization and improvement of existing processes.
In addition, you will be involved in maintaining the GCO Quality Management System (e.g. documenting change requests, tracking the review and approval of new document versions, sharing related information with the team). You will also support the department in gathering information on all relevant topics within and outside our organization, as well as distributing information within GCO.
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At Teva
Assoc Dir Clinical Development
Miha Pongrac
Human Resources
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