Regulatory Programs Lead
3 days ago
As a Senior Global Program Regulatory Manager at Novartis, you will be responsible for developing and implementing the global regulatory strategy for programs through development, registration, and post-approval in assigned regions. You may act as the RA program lead on programs of limited complexity.
This role offers hybrid working, requiring 3 days a week / 12 days a month based in office.
You will work with limited supervision to provide input to global program regulatory strategy, including regulatory designations & innovative approaches. You may also provide global RA leadership for a specific part of the program or act as lead for a program of limited complexity.
Key Responsibilities- Provide strategic input into cross-functional deliverables
- Coordinate regulatory readiness with other line functions, Country Organizations & Regions
- Contribute to the development and maintenance of key documents
- Science-based bachelor's or advanced degree
- Advanced understanding of pharmaceutical development, clinical trials
- Fluency in English
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