[All remote jobs](https://jobicy.com/jobs.md)[![Jade Biosciences logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2026/11/07b1366a60be-221.webp)](https://jobicy.com/company/jade-biosciences.md)[Jade Biosciences](https://jobicy.com/company/jade-biosciences.md) # Executive Director, Clinical Supply Management AI Summary Jade Biosciences is seeking an Executive Director to lead and scale its Clinical Supply Management function across a portfolio of biologic programs. The role owns global clinical supply strategy, forecasting, CMO and logistics oversight, IRT/IxRS planning, budget management, and supply-risk reporting. It requires deep expertise in cold-chain biologics, multi-country Phase 3 studies, regulatory compliance, and preparation for BLA filing and commercial launch. The executive will build an internal and external operating model while aligning CMC, Clinical Operations, Quality, Regulatory Affairs, and development stakeholders. This is a remote leadership position with periodic travel to company and team events.[Apply for this job](#job-application)[View company](https://jobicy.com/company/jade-biosciences.md)ShareRemote from[USA](https://jobicy.com/job-region/usa.md), [Canada](https://jobicy.com/job-region/canada.md)SalaryUSD 280k–300k / yrDepartment[Product & Operations](https://jobicy.com/categories/management.md)EmploymentFull TimeExperienceDirectorPublished12 Nov 2026Apply before12 Dec 2026Listing views41Application actions2Application toolkit ## Make your next move. Prepare your resume, explore your fit, and draft a cover letter for this opportunity. Opportunity details ## About this role. About [Jade Biosciences](https://jobicy.com/company/jade-biosciences.md) Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade’s lead candidate, JADE101, targets the cytokine APRIL, and is currently being evaluated for the treatment of immunoglobulin A nephropathy. Jade’s pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an anti-IFN-β monoclonal antibody. Jade was launched based on assets licensed from Paragon Therapeutics, an antibody discovery engine founded by Fairmount. For more information, visit [JadeBiosciences.com](https://url.usb.m.mimecastprotect.com/s/kwQpCrgGLMHxLkBujt66i4Vdxs?domain=globenewswire.com) and follow the Company on [LinkedIn](https://url.usb.m.mimecastprotect.com/s/S9DbCvmMP9TvMYkC5ulliQtFaR?domain=globenewswire.com). Role Overview Jade is developing potentially transformational, disease-modifying therapies for people living with autoimmune diseases. With three biologics programs in the clinic and multiple ongoing studies from Phase I to Phase III, we are seeking an experienced Executive Director, Clinical Supply Management to join our CMC leadership team and make sure every patient in our trials receives the right investigational product, on time. Reporting to the Chief Technology Officer (Head of CMC), you will own clinical supply strategy, planning and execution for all Jade programs. You will shape and scale the Clinical Supply Management function, growing and mentoring a team of internal employees and contractors, and you will lead a global network of CMOs and logistics partners supporting complex, multi-country and multi-site studies with ambitious timelines and enrollment targets. This is a high-impact role for a self-starter who combines strategic thinking with hands-on execution. You will work closely with Clinical Operations and Clinical Development to secure supply for every planned study, help prepare the supply chain for BLA filing, launch and commercial readiness, and contribute directly to Jade’s key corporate goals. Key Responsibilities * Lead and build the function: Provide strategic and operational leadership for Jade’s Clinical Supply Management function. Further develop and scale the team through a combination of internal headcount and external partners, including recruiting, onboarding and mentoring team members and consultants. Develop robust business processes and SOP in close collaboration with the Quality function. * Define the clinical supply strategy: Develop and implement the clinical supply strategy for all Jade programs, from early-stage (Phase 1/2) through late-stage (Phase 3) development, with a forward-looking view toward BLA filing, product launch and commercial readiness. * Plan demand and supply: Build and maintain integrated global demand forecasts and supply plans based on protocols, enrollment projections and site activation plans. Balance drug product availability, shelf life, overage and cost, and update plans as studies evolve. Advise on potential risk and challenges to Senior Management and peer groups such as Clinical Operations and Development. * Collaborate cross-functionally: Partner closely with Clinical Operations and Clinical Development on study-specific supply strategies, and with Quality, Regulatory Affairs and CMC to forecast, align and continuously update supply requirements for ongoing and future studies. Develop options and recommendations for stakeholders and senior management. * Select and manage CMOs and suppliers: Select, contract and manage clinical supply CMOs, depots, couriers, logistics providers, and other critical suppliers. Set clear performance expectations and KPIs, and build strong partnerships that ensure quality, reliability and cost-effective supply. * Oversee clinical supply operations: Direct labeling, packaging, blinding, cold-chain storage and global distribution for all drug product formats, including vials, pre-filled syringes and autoinjectors. Manage comparator sourcing, expiry extensions, relabeling, returns, reconciliation and destruction. * Manage IRT and inventory: Define supply requirements for IRT/IxRS systems, including resupply strategies and user acceptance testing, and monitor inventory at depots and sites to prevent stock-outs and minimize waste. * Ensure compliance and quality: Maintain full compliance with Jade SOPs, cGMP, GDP, GCP, ICH guidelines and applicable global regulatory and import/export requirements. Partner with Quality on batch release (including QP release for EU studies), deviations and change controls, keep the function inspection-ready, and contribute to regulatory submissions (IND, IMPD, CTA). * Own the budget and reporting: Manage the clinical supply budget, and report regularly and concisely to stakeholders and senior management on inventory, supply and demand, changes and risks across all programs. Qualifications * Bachelor’s or Master’s degree (or equivalent) in Life Sciences, Chemical Engineering or a related field. * 15+ years of progressive experience in clinical supply chain management, ideally with biologics, including significant experience leading teams. Experience in commercial supply chain management is a plus. * Proven experience managing clinical supply for biologics in vials within cold-chain environments, using local and multinational CMOs; experience with pre-filled syringes and combination products such as autoinjectors highly preferred. * Experience supporting multiple early- and late-stage programs, including multi-country Phase 3 studies and bridging studies for biologic combination products. * Comprehensive understanding of global regulatory and import/export requirements across Europe, North America, China, Japan and Rest of World (ROW), and strong working knowledge of cGMP, GDP and GCP. * Hands-on experience with IRT/IxRS systems, clinical supply forecasting tools and budget management. * Demonstrated success building and scaling clinical supply functions, including hiring, onboarding and managing team members and consultants to meet critical milestones. * Exceptional communication, leadership and interpersonal skills, with a track record of aligning CMC, Quality, Regulatory Affairs and Clinical teams and building trusting relationships with external CMO partners. * A strategic thinker with a proven execution record, strong problem-solving skills and the ability to thrive in a complex, fast-paced clinical development environment. Position Location This is a remote role; periodic travel to team and company events is required. The anticipated salary range for candidates for this role is $280,000 – $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. 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](https://www.e-verify.gov/sites/default/files/everify/images/manuals/EVParticipationPoster.JPG). 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. Show more [Apply now >](https://jobicy.com/jobs/161594-executive-director-clinical-supply-management.md) * ![Upload CV](data:image/svg+xml;base64,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) ### Upload your resume now To unlock remote work opportunities and be discovered by global employers. This job listing has been manually reviewed by the Jobicy Trust & Safety Team for compliance with our posting guidelines, including verification of the company's legitimacy, accuracy of job details, clarity of remote work policy, and absence of misleading or fraudulent content. ## Role DNA A quick view of the complexity, pace, ownership and collaboration implied by the job description. ### Job Complexity 5/5EasyHard ### Pace & Pressure 5/5RelaxedFast-paced ### Autonomy Level 5/5GuidedFull ownership ### Communication Load 5/5IndependentCollaborative AI insightThis is a highly complex executive role requiring 15+ years of clinical supply experience and accountability for uninterrupted global investigational-product supply. The leader must balance operational execution, regulatory compliance, supplier performance, budgets, and high-stakes clinical timelines across multiple programs. ## Salary analysis Estimated compensation compared with the broader US market for similar roles. Estimated job median (per year)Market rate$290,000US market range (per year)$250k–$340k0$374.00k AI insightThe yearly pay period is inferred from the job context; it was not explicitly stated by the employer. The employer discloses a base salary range of USD 280,000 to USD 300,000. The annual cadence is inferred from the compensation magnitude and the senior executive biotechnology role, as the posting does not explicitly state a pay period. A reasonable estimated US market range for a comparable clinical supply executive is USD 250,000 to USD 340,000 per year. ## Core skills Skills and capabilities most closely associated with this opportunity. [Clinical Supply Management](https://jobicy.com/jobs?search_keywords=Clinical%20Supply%20Management.md)[Clinical Supply Chain Strategy](https://jobicy.com/jobs?search_keywords=Clinical%20Supply%20Chain%20Strategy.md)[Biologics Supply Chain](https://jobicy.com/jobs?search_keywords=Biologics%20Supply%20Chain.md)[Cold Chain Logistics](https://jobicy.com/jobs?search_keywords=Cold%20Chain%20Logistics.md)[Demand Forecasting](https://jobicy.com/jobs?search_keywords=Demand%20Forecasting.md)[Supply Planning](https://jobicy.com/jobs?search_keywords=Supply%20Planning.md)[CMO Management](https://jobicy.com/jobs?search_keywords=CMO%20Management.md)[IRT/IxRS](https://jobicy.com/jobs?search_keywords=IRTIxRS.md)[cGMP Compliance](https://jobicy.com/jobs?search_keywords=cGMP%20Compliance.md)[GDP Compliance](https://jobicy.com/jobs?search_keywords=GDP%20Compliance.md)[Clinical Trial Operations](https://jobicy.com/jobs?search_keywords=Clinical%20Trial%20Operations.md)[Global Distribution](https://jobicy.com/jobs?search_keywords=Global%20Distribution.md)[Budget Management](https://jobicy.com/jobs?search_keywords=Budget%20Management.md)[Regulatory Submissions](https://jobicy.com/jobs?search_keywords=Regulatory%20Submissions.md)[Team Leadership](https://jobicy.com/jobs?search_keywords=Team%20Leadership.md) Sample interview questionsHow would you build a clinical supply strategy for programs progressing from Phase 1 through Phase 3?I would begin with an integrated product and protocol roadmap covering demand assumptions, enrollment scenarios, site activation, shelf life, manufacturing capacity, labeling, and distribution requirements. I would establish scenario-based forecasts, governance routines, and risk registers, then refresh them regularly with Clinical Operations, CMC, Quality, and Regulatory Affairs as program assumptions evolve. Describe your approach to preventing stock-outs while controlling investigational product waste. I use IRT-driven resupply parameters supported by site-level consumption data, enrollment forecasts, depot inventory visibility, and lead-time analysis. I set safety-stock thresholds according to patient risk and supply constraints, monitor expiry closely, and use planned redistribution, relabeling, or expiry-extension strategies where compliant and appropriate. What criteria do you use to select and manage CMOs and clinical logistics providers? I assess technical fit, capacity, quality history, cold-chain capability, geographic reach, inspection readiness, financial stability, responsiveness, and total cost. After selection, I define quality agreements, KPIs, escalation paths, meeting cadence, and contingency plans to ensure transparent performance management and dependable execution. How would you prepare the clinical supply organization for BLA filing and commercial readiness? I would create a phased readiness plan that strengthens supply planning, comparability and stability data management, supplier qualification, quality systems, batch-release processes, and documentation needed for regulatory submissions. I would also align clinical and commercial supply assumptions early to identify capacity, packaging, and distribution risks before launch-critical decisions are required. How do you communicate supply risks to senior leadership and cross-functional stakeholders? I communicate risks through concise, decision-oriented reporting that explains the issue, probability, patient and timeline impact, mitigation options, owner, and decision deadline. 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