Full-Time Senior Medical Director, Alzheimer's Disease
Biogen is hiring a remote Full-Time Senior Medical Director, Alzheimer's Disease. The career level for this job opening is Senior Manager and is accepting Remote based applicants remotely. Read complete job description before applying.
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About This Role: As a Senior Medical Director for Alzheimer’s disease & Dementia (ADD) Clinical Development, you will lead pioneering programs to transform lives. You'll lead and oversee clinical development activities across early and late-stage programs. This role requires scientific acumen, strategic planning, and leadership to advance clinical assets from discovery through regulatory approval and post-market surveillance.
What You’ll Do:
- Lead strategic framework for clinical development plans, aligning scientific rationale, regulatory requirements, product development, and commercial objectives.
- Implement and manage the Clinical Development Plan for the ADD clinical pipeline and research assets.
- Guide clinical development from early-stage assets through registration and post-approval phases.
- Offer clinical expertise for early development assets, supporting the transition from research to development (R2D).
- Provide clinical insights for partnered assets and support due diligence for potential external assets.
- Serve as the Development Lead for an asset.
- Be an active member of the functional leadership team, influencing senior cross-functional counterparts.
- Engage with global regulatory authorities and foster relationships that facilitate the clinical development process.
Who You Are: You are a visionary leader with an MD or MD/PhD, ideally grounded in neurodegeneration or movement disorders. Your past five years have shown successes in pharmaceutical clinical development, including leading registration-stage programs and navigating global regulatory interactions. You are experienced with business development and due diligence processes. Experience with rare indications is a plus.
Required Skills:
- MD or MD/PhD with specialization in relevant fields (neurology, neurodegeneration, etc.)
- Minimum 5 years of experience in the pharmaceutical industry
- Proven track record of leading clinical programs to submission and approval
- Demonstrable experience with filing INDs
- Extensive interaction with global regulatory authorities
- Proficiency in business development and due diligence