Vice President, Medical Affairs

Posted Aug 27

This is a fully remote position, open to applicants in United States.

πŸ“‹ Description

β€’ Lead and develop the medical affairs function at Jade Biosciences as its pipeline progresses through late-stage development and commercialization.

β€’ Formulate and implement the medical affairs strategy for JADE101, JADE201, and JADE301, with an initial focus on JADE101 in IgA nephropathy.

β€’ Act as a scientific and clinical advisor to the Chief Medical Officer, as well as to clinical development, regulatory, and clinical operations teams.

β€’ Cultivate relationships with key opinion leaders, investigators, patient advocacy groups, and professional societies in the fields of nephrology and immunology/rheumatology.

β€’ Facilitate advisory boards, scientific exchanges, and congress strategies.

β€’ Represent Jade externally as a medical and scientific authority.

β€’ Oversee evidence-generation initiatives, including real-world evidence and investigator-sponsored studies.

β€’ Manage the publication strategy.

β€’ Supervise medical communications, publications, and medical information resources.

β€’ Ensure the medical organization is prepared for product launches.

β€’ Guarantee that medical affairs activities adhere to all relevant laws, regulations, and industry standards.

β€’ Collaborate with clinical operations, regulatory, biometrics, and commercial teams on an integrated program strategy.


⛳️ Requirements

β€’ MD degree is required.

β€’ Board certification and/or relevant post-graduate clinical training is highly preferred.

β€’ A minimum of 10 years of experience in the biopharmaceutical industry, with progressive leadership roles in medical affairs and/or clinical development.

β€’ Proven track record in establishing or leading medical affairs functions, including field medical teams, within a clinical-stage or commercial organization.

β€’ Demonstrated ability to engage effectively with key opinion leaders, investigators, and external scientific stakeholders.

β€’ In-depth knowledge of the regulatory, compliance, and legal frameworks governing medical affairs activities.

β€’ Exceptional skills in scientific communication, leadership, and cross-functional collaboration.

β€’ Experience in renal (nephrology) β€” for instance, IgA nephropathy or other glomerular diseases β€” is a significant advantage.

β€’ Familiarity with immunology/rheumatology and knowledge of B-cell and autoantibody-driven autoimmune diseases is a strong plus.

β€’ Experience in supporting late-stage development and/or product launches in rare or specialty autoimmune indications is desirable.

β€’ Understanding of biologics/monoclonal antibody therapeutics and biomarker-driven development is beneficial.

β€’ Occasional travel for team and company events is required.

β€’ Authorization to work in the United States must be verified through I-9 and E-Verify.


🏝️ Benefits

β€’ Comprehensive health and welfare benefits.

β€’ 401(k) plan with company contribution.

β€’ Paid time off.

β€’ Competitive compensation package that includes a base salary.

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