About this role:

As the Director, US Regulatory Lead you are responsible for all aspects of the US Regulatory Strategy for the assigned development products. You are a critical member of the Regulatory Product Team providing US focused product development strategy and analyzing the impact of relevant external regulatory initiatives. You will serve as the point of contact for the Agency’s interactions. You will also partner with the Global Regulatory Lead (GRL) and will participate on cross-functional project teams representing the regulatory function on an agenda driven basis. Additionally, you will present the US regulatory position on assigned products to senior management governance committees as needed. Externally, you may participate and/or lead a variety of US focused Trade Association initiatives.

 What You’ll Do:

·       Core member of the Regulatory Project team working collaboratively to weave US strategies into global strategies as they are developed.

·       Key contact for FDA on product(s) and with direct FDA interaction.

·       Ensure communications from the FDA are properly communicated to the business after assessing the feedback and outlining next steps.

·       Drive the US product labeling and work with the GRL to ensure core label changes are appropriately conveyed in US product labeling.

·       Partner with US Commercial and Ad Promo Team.

·       Responsible for IND and BLA submissions to FDA in partnership with Regulatory Operations.

·       Regulatory representative on due diligence assessments of new business opportunities as required.

·       Provide mentorship to junior regulatory staff.

Who You Are:

In addition to having exceptional relationship building with the agencies, you successfully worked in a matrix environment where you collaborated with other teams within the organization. You have strong US Regulatory experience along with strong teamwork capabilities.

#LTD-1

Required Skills

·       8+ years’ experience in the pharmaceutical industry within R&D, Regulatory or a related function, with at least 5 years working in regulatory affairs.

·       Delivery of at least one major application (NDA or BLA) or extensive experience with late-stage development preferred.

·       Experience working with the FDA (ideally both with CBER and CDER)

·       Great leadership skills with high emotional intelligence.

·       Must be a great team player with strong verbal and written communication skills.

Why Biogen?

Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients’ lives and on changing the course of medicine. Together, we pioneer. Together, we thrive.