Lifecycle Management Strategy Lead - Friedreich Ataxia

Job Description

About This Role

To support value creation, we established a Product Development and Commercialization (PDC) Team. Having made the first approved treatment for Friedreich Ataxia available in the US, Germany and 20 further countries to date, PDC priorities include geographic expansion and launch in collaboration with the affiliates/regions, executing a robust evidence generation plan and life-cycle management (LCM).

The role of this Lifecycle Management (LCM) Strategy Lead - Friedreich Ataxia is to work in particular across Research, Development, Regulatory, Clinical Operations, Biomarkers, Medical and Corporate Affairs functions as part of the PDC team, reporting to the PDC Lead. The LCM Strategy Lead will operate with senior leaders in each key PDC function and help to facilitate therapeutic area and asset growth in this highly matrixed environment. The role is based in Cambridge, Massachusetts, USA Headquarters.

What You’ll Do

• Execute and evolve the disease area and asset strategy for life-cycle management, for example the development and implementation of new studies (e.g., Pediatric Study), formulations, novel biomarkers, patient management support strategies, and other drivers of near- and longer-term growth 
• Develop a global KME management plan that expands PDC engagement for LCM feedback beyond the core group of experts the regions depend upon
• Lead PDC strategic team to define the external communications strategy for FA, based on 360-degree view of the competitive landscape. Triage externally generated data for internal communication and guidance
• Develop compelling business cases and engage cross-functional experts to develop recommendations for PDC endorsement from executive management
• Drive the Disease Area Strategic Plan and Long-Range Forecast processes

Who You Are

You are a leader, a strategic thinker with the energy and vision to succeed in a fast paced and complex environment. You have experience and are passionate about driving positive change for patient with rare diseases. Based on your strong expertise in either R&D, business development, commercial or corporate strategy, you are used to driving and leading cross-functional collaboration at all levels and to influence and guide senior stakeholders.

Qualifications

• 10+ years of experience in pharma, biotech or consulting; rare disease experience strongly preferred
• Bachelor’s degree required and Master’s degree preferred.
• Demonstrated ability to lead through influence, navigate in ambiguity and deliver results
•  Strong Science background; robust knowledge of clinical trial design and regulatory engagement preferred
• Strong track record of executing LCM strategies to support asset growth goals
• Robust scientific understanding w/ ability to extract insights for competitive differentiation and strategic planning
• Advanced analytical competencies; ability to develop business cases for investment

Additional Information

All your information will be kept confidential according to EEO guidelines.

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.