Transform patient lives as a Senior Manager of Global Regulatory Strategy at Bristol Myers Squibb. Drive innovative solutions and navigate regulatory complexities in a meaningful role that shapes patient access to therapies.
As a Senior Manager, you will collaborate closely with regional strategists and the GRL Team leader to develop strategic plans for product registration in Neurosciences. This role requires at least two years of regulatory experience, along with a strong background in drug development and FDA guidelines. You will lead the preparation of regulatory submissions and develop strategies to resolve challenges effectively.
Key Responsibilities:
• Develop strategic operational plans for product registration
• Lead content creation for US regulatory submissions
• Create contingency plans for regulatory objectives
• Address regulatory issues to facilitate patient access
• Build relationships with health authorities for effective collaborations
Requirem...