Associate Director, Global Labeling Lead

About This Role

The purpose of the Global Labeling group is to drive Biogen's regulatory labeling strategy and ensure that labeling documents are of high quality and compliant for the safe and effective use of our products globally.

As a Global Labeling Associate Director, you would be responsible for developing the labeling strategy, leading the development and update of core, EU and US labeling documents and for overseeing implementation at a regional and local level. In this role, you may be responsible for overseeing the strategy for other products within your Therapeutic Area.

What You'll Do

• Lead timely creation or management of regulatory compliant, competitive and up to date core, EU and US labeling documents throughout the product lifecycle including the Target Label Profile, Core Data Sheet, EU SmPC and USPI
• Lead the cross functional product Labeling Team to reach consensus on labeling matters, accurately capture and communicate decisions, and obtain endorsement by senior management
• Critically assess the data and propose the labeling strategy to be followed in core, EU and US labeling documents, ensuring alignment with global, regional and local regulatory strategies
• Oversee distribution and tracking of Core Data Sheet updates for assigned products, ensuring compliance is maintained within the Electronic Document Management System and the Regulatory Tracking System
• Understand scientific concepts to critically assess clinical data, enable proactive interactions with appropriate stakeholders, influence the clinical development plan
• Develop and implement strategy for global, EU and US labeling content
• Identify underlying processes and principles for developing product claims representing the risks and opportunities to the project team
• Partner with key stakeholders to ensure product labeling is the most current, accurate, relevant and competitive to inform prescribers and patients

• Bachelor's degree in a scientific or medically related discipline
• 6+ years pharmaceutical/ biotechnology industry regulatory experience, including global, EU and US regulatory labeling
• Advanced knowledge and understanding of applicable regulations, pharmacology, medicine, pharmacovigilance and drug development
• Experience in interpretation of global, EU and US regulations, guidelines, policy statements, etc.
• Proven ability to successfully understand regulatory implications of product strategy with regard to the product label, assessment and practical management of associated impacts
• Demonstrate effective cross-functional and cross-cultural skills to effectively interact with global counterparts
• Well organized, detail oriented, highly effective written and oral communication skills

• Medical, Dental, Vision, & Life insurances
• Fitness & Wellness programs including a fitness reimbursement
• Short- and Long-Term Disability insurance
• A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
• Up to 12 company paid holidays + 3 paid days off for Personal Significance
• 80 hours of sick time per calendar year
• Paid Maternity and Parental Leave benefit
• 401(k) program participation with company matched contributions
• Employee stock purchase plan
• Tuition reimbursement of up to $10,000 per calendar year
• Employee Resource Groups participation