- ctions as required by regulatory agencies including adverse events data from
- clinical trials, spontaneous or solicited sources, periodic and experience reports.
- May provide trending and safety signal detection and assessment.
- Supports all clinical trial activity and post marketing.
Minimum requirements
- Operations Management and Execution
- Collaborating across boundaries
- Functional Breadth
Pour postuler à ce poste veuillez visiter ce lien: https://www.novartis.com/careers/career-search/job-details/300726BR
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