Opportunity Description
Advance medical innovation as a Senior Manager of Regulatory Affairs in Neurosciences at Bristol Myers Squibb. Lead strategic initiatives to influence regulatory pathways and improve patient access to cutting-edge therapies.
As a key player in this role, you will collaborate with teams to create regulatory strategies and content necessary for product registrations. This position necessitates a strong scientific educational background and at least two years of relevant regulatory experience. Your contributions will focus on resolving regulatory issues and managing health authority interactions to ensure timely approvals.
Key Responsibilities:
• Develop and lead regulatory strategy for product registration
• Prepare responses to health authority inquiries
• Track public-private regulatory meetings and workshops
• Contribute to key development documents
• Identify and compile regulatory lessons learned
Requirements:
• Ph.D., M.D., PharmD, MS, or BS in a relevant...
As a key player in this role, you will collaborate with teams to create regulatory strategies and content necessary for product registrations. This position necessitates a strong scientific educational background and at least two years of relevant regulatory experience. Your contributions will focus on resolving regulatory issues and managing health authority interactions to ensure timely approvals.
Key Responsibilities:
• Develop and lead regulatory strategy for product registration
• Prepare responses to health authority inquiries
• Track public-private regulatory meetings and workshops
• Contribute to key development documents
• Identify and compile regulatory lessons learned
Requirements:
• Ph.D., M.D., PharmD, MS, or BS in a relevant...
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