Vice President, Medical Affairs

Posted 1hrs ago

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Job Description

Medical affairs executive building strategy and capabilities for Jade Biosciences’ autoimmune disease pipeline. Advancing JADE101 and subsequent therapies through development and launch readiness.

Responsibilities:

  • Build and lead Jade Biosciences’ medical affairs function as its pipeline advances through late-stage development and commercialization
  • Define and execute the medical affairs strategy across JADE101, JADE201, and JADE301, initially emphasizing JADE101 in IgA nephropathy
  • Serve as a scientific and clinical thought partner to the Chief Medical Officer, clinical development, regulatory, and clinical operations
  • Establish relationships with key opinion leaders, investigators, patient advocacy groups, and professional societies in nephrology and immunology/rheumatology
  • Lead advisory boards, scientific exchange, and congress strategy
  • Represent Jade externally as a medical and scientific voice
  • Direct evidence-generation activities, including real-world evidence and investigator-sponsored studies
  • Lead publication strategy
  • Oversee medical communications, publications, and medical information resources
  • Ensure launch readiness of the medical organization
  • Ensure medical affairs activities comply with applicable laws, regulations, and industry codes
  • Partner with clinical operations, regulatory, biometrics, and commercial teams on integrated program strategy

Requirements:

  • MD required
  • Board certification and/or relevant post-graduate clinical training strongly preferred
  • 10+ years of biopharmaceutical industry experience, with progressive leadership responsibility in medical affairs and/or clinical development
  • Demonstrated success building or leading medical affairs functions, including field medical teams, in a clinical-stage or commercial organization
  • Proven ability to engage credibly with key opinion leaders, investigators, and external scientific stakeholders
  • Strong knowledge of the regulatory, compliance, and legal frameworks governing medical affairs activities
  • Excellent scientific communication, leadership, and cross-functional collaboration skills
  • Renal (nephrology) experience — e.g., IgA nephropathy or other glomerular diseases — is a strong plus
  • Immunology / rheumatology experience and familiarity with B-cell– and autoantibody-driven autoimmune diseases is a strong plus
  • Experience supporting late-stage development and/or product launch in a rare or specialty autoimmune indication
  • Familiarity with biologics/monoclonal antibody therapeutics and biomarker-driven development
  • Periodic travel to team and company events is required
  • Authorization to work in the United States is verified through I-9 and E-Verify

Benefits:

  • Health and welfare benefits
  • 401(k) with company contribution
  • Paid time off
  • Comprehensive compensation package including base salary