Job Description
Responsible for all activities of Japan regulatory operations as a lead of regulatory operation in collaboration with Global RA, Japan R&D, and other functional areas within Biogen.
Manage and maintain regulatory operational activities in drug development, NDA filing, NDA review, and post marketing stages (e.g., CTN, NDA/sNDA, JPI) in Japan based on the depth knowledge on Japanese regulation.
Develop and maintain procedures necessary to perform JRA activities in compliance with regulatory affairs and global policy/SOP
Support to maintain marketing business licenses in Japan according to the regulation
Key Responsibilities:
Qualifications
Essential Skills and Qualifications Required:
Education:
Experience:
Additional Information
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.
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
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