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Senior Medical Director, Alzheimer’s Disease & Dementia, Clinical Development

Biogen
Full-time
Remote friendly (United States)
United States
$268,000 - $369,000 USD yearly
Clinical Research and Development

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Role Summary

Senior Medical Director for Alzheimer’s disease & Dementia (ADD) Clinical Development, leading and overseeing clinical development activities across early and late-stage programs within Biogen's ADD portfolio. Responsible for developing and implementing Clinical Development Plans (CDPs) to meet timelines and ensure progression criteria, while shaping the ADD pipeline through cross-functional collaboration and oversight of research assets, partnerships, and due diligence.

Responsibilities

  • Lead the 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 to registration and post-approval phases.
  • Offer clinical expertise for early development assets during the research phase, 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, contributing to broader strategy discussions and influencing senior cross-functional counterparts.
  • Engage with global regulatory authorities and foster relationships that facilitate the clinical development process.

Qualifications

  • MD or MD/PhD with specialization in neurology, neurodegeneration, geriatric neurology, neurocognitive disorders or movement disorders.
  • Minimum of 5 years of experience in the pharmaceutical industry.
  • Proven track record of leading clinical programs to regulatory submission and approval stages.
  • Demonstrable experience with filing Investigational New Drug applications (INDs).
  • Extensive interaction with global regulatory authorities.
  • Proficiency in business development and due diligence activities.

Skills

  • Strategic thinking and exceptional problem-solving skills.
  • Strong leadership and team management abilities.
  • Excellent communication and interpersonal skills, capable of fostering collaborative relationships.

Education

  • Not specified

Additional Requirements

  • Travel requirements or physical demands are not specified as part of essential job duties in the provided content.