Jade Biosciences
Medical Director (Nephrology)
Jade Biosciences, San Francisco, California, United States, 94199
About Jade Biosciences
Jade Biosciences is focused on developing innovative, best-in-class therapies to address critical unmet needs in autoimmune diseases. Our lead candidate, JADE101, is designed to inhibit the cytokine APRIL (A Proliferation‑Inducing Ligand) and is being developed for the treatment of immunoglobulin A nephropathy (IgAN), a chronic kidney disease that can impair kidney function over time. JADE101 aims to reduce harmful IgA antibodies, lower proteinuria (a key marker of kidney damage), and preserve long‑term kidney function. A Phase 1 healthy‑volunteer study of JADE101 is ongoing, with interim, biomarker‑rich data expected in the first half of 2026. Jade’s pipeline also includes a second development candidate, JADE201, and an undisclosed antibody discovery program, JADE-003, both currently in preclinical development. For more information, visit JadeBiosciences.com and follow us on LinkedIn.
Role Overview We are seeking an experienced and mission‑driven Medical Director to lead and support clinical programs in nephrology, with a focus on rare or immune‑mediated kidney diseases. This role is ideal for a physician‑scientist who thrives in a small biotech environment where agility, cross‑functional collaboration, and scientific leadership are essential. The Medical Director will play a key role in advancing Jade’s pipeline through clinical development. This newly created position will report to the Executive Medical Director of Clinical Development. This is a fully remote role and will require some travel.
Key Responsibilities
Clinical Development
Lead the design, execution, and oversight of clinical trials in nephrology, including protocol development, study monitoring, and data interpretation.
Serve as Medical Monitor for ongoing trials, ensuring patient safety and scientific integrity.
Collaborate with clinical operations, regulatory, and biometrics teams to ensure trial success and compliance.
Educate and advise clinical sites/investigators to support enrollment and optimal study conduct, including presenting at investigator meetings and/or site initiation visits, and serving as the medical point of contact for site staff questions about patient eligibility, and providing input into patient safety assessment and management.
Provide medical expertise and support to external partners, vendors, and contractors as required to ensure smooth program execution.
Communicate effectively, orally and in writing, with internal and external stakeholders regarding the assigned clinical program, including the CMO, CEO, external medical experts and others.
Regulatory and Scientific Contributions
Contribute to the preparation of regulatory documents (INDs, NDAs, briefing documents, etc.).
Support interactions with regulatory authorities and ethics committees.
Stay current with scientific literature and competitive landscape in nephrology and related fields.
Cross‑Functional Collaboration
Partner with translational science, biomarker, and commercial teams to align clinical strategy with broader company goals.
Provide medical input into lifecycle planning and early market preparation.
Stakeholder Engagement
Begin building relationships with key opinion leaders (KOLs), investigators, and advocacy groups in nephrology.
Represent the company at scientific meetings, advisory boards, and industry events.
Qualifications
MD (or equivalent medical degree); board certification in nephrology strongly preferred.
3+ years of experience as a nephrologist in academia or industry, and/or experience in nephrology clinical trials or rare disease programs.
Experience in clinical trial design, execution, and medical monitoring.
Strong clinical judgment, scientific rigor, and regulatory knowledge.
Ability to work independently and thrive in a fast‑paced, matrixed environment.
Ability to manage multiple projects simultaneously and prioritize effectively in a fast‑paced environment.
Strong analytical, problem‑solving, and decision‑making skills.
Excellent communication and interpersonal skills with the ability to influence and motivate cross‑functional teams, manage a diverse set of stakeholders, and work closely with team leaders.
High ethical standards and impeccable integrity.
Exercise sound judgment in managing complex, confidential, and regulated information.
Position Location This is a remote role; periodic travel to scientific conferences, sites, team and company events is required.
Salary The anticipated salary range for candidates for this role is $270,000-$300,000. The final salary offered will depend on several factors, which may include, but not limited to, relevant years of experience, educational background, and geography.
Equal Opportunity Employer Jade Biosciences is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.
As part of the I‑9 verification of authorization to work in the United States, Jade Bioscience participates in E‑Verify. To learn more about E‑Verify please review this poster.
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Role Overview We are seeking an experienced and mission‑driven Medical Director to lead and support clinical programs in nephrology, with a focus on rare or immune‑mediated kidney diseases. This role is ideal for a physician‑scientist who thrives in a small biotech environment where agility, cross‑functional collaboration, and scientific leadership are essential. The Medical Director will play a key role in advancing Jade’s pipeline through clinical development. This newly created position will report to the Executive Medical Director of Clinical Development. This is a fully remote role and will require some travel.
Key Responsibilities
Clinical Development
Lead the design, execution, and oversight of clinical trials in nephrology, including protocol development, study monitoring, and data interpretation.
Serve as Medical Monitor for ongoing trials, ensuring patient safety and scientific integrity.
Collaborate with clinical operations, regulatory, and biometrics teams to ensure trial success and compliance.
Educate and advise clinical sites/investigators to support enrollment and optimal study conduct, including presenting at investigator meetings and/or site initiation visits, and serving as the medical point of contact for site staff questions about patient eligibility, and providing input into patient safety assessment and management.
Provide medical expertise and support to external partners, vendors, and contractors as required to ensure smooth program execution.
Communicate effectively, orally and in writing, with internal and external stakeholders regarding the assigned clinical program, including the CMO, CEO, external medical experts and others.
Regulatory and Scientific Contributions
Contribute to the preparation of regulatory documents (INDs, NDAs, briefing documents, etc.).
Support interactions with regulatory authorities and ethics committees.
Stay current with scientific literature and competitive landscape in nephrology and related fields.
Cross‑Functional Collaboration
Partner with translational science, biomarker, and commercial teams to align clinical strategy with broader company goals.
Provide medical input into lifecycle planning and early market preparation.
Stakeholder Engagement
Begin building relationships with key opinion leaders (KOLs), investigators, and advocacy groups in nephrology.
Represent the company at scientific meetings, advisory boards, and industry events.
Qualifications
MD (or equivalent medical degree); board certification in nephrology strongly preferred.
3+ years of experience as a nephrologist in academia or industry, and/or experience in nephrology clinical trials or rare disease programs.
Experience in clinical trial design, execution, and medical monitoring.
Strong clinical judgment, scientific rigor, and regulatory knowledge.
Ability to work independently and thrive in a fast‑paced, matrixed environment.
Ability to manage multiple projects simultaneously and prioritize effectively in a fast‑paced environment.
Strong analytical, problem‑solving, and decision‑making skills.
Excellent communication and interpersonal skills with the ability to influence and motivate cross‑functional teams, manage a diverse set of stakeholders, and work closely with team leaders.
High ethical standards and impeccable integrity.
Exercise sound judgment in managing complex, confidential, and regulated information.
Position Location This is a remote role; periodic travel to scientific conferences, sites, team and company events is required.
Salary The anticipated salary range for candidates for this role is $270,000-$300,000. The final salary offered will depend on several factors, which may include, but not limited to, relevant years of experience, educational background, and geography.
Equal Opportunity Employer Jade Biosciences is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.
As part of the I‑9 verification of authorization to work in the United States, Jade Bioscience participates in E‑Verify. To learn more about E‑Verify please review this poster.
#J-18808-Ljbffr