Senior Manager, Clinical Supply Chain Management

Kiniksa Pharmaceuticals is a commercial‑stage biopharmaceutical company developing and commercializing novel therapies for diseases with unmet need, with a focus on cardiovascular indications. With deep expertise in immunology and inflammation, Kiniksa is advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST, the first and only FDA‑approved therapy for recurrent pericarditis. Grounded in rigorous science and bold innovation, the company fosters a highly collaborative, patient‑first culture led by accomplished life sciences leaders. At Kiniksa, talented individuals are trusted and empowered to make a real impact—shaping the future of medicine while improving the lives of patients who need it most.Reporting to the Sr. Director, Clinical Supply Chain, the Senior Manager, Clinical Supply Chain Management will provide operational leadership and cross-functional coordination for end-to-end clinical supply activities across assigned clinical studies and programs. This role is responsible for ensuring reliable supply, proactively identifying and mitigating risks, and supporting alignment with Clinical Operations, Quality, Regulatory, CMC/Manufacturing, and external partners. Successful candidates bring a hands-on, solutions-oriented mindset, demonstrate strong judgment and accountability, and thrive in a dynamic, fast-paced environment.This is an office-based role at our office located in Lexington, Ma. Our office-based employees follow a schedule of 5 days in the office.Responsibilities (including, but not limited to):Provide end-to-end clinical supply support to ensure continuous supply of clinical trial material for assigned studies globallyEnsure on-time startup and ongoing execution of new studies by aligning supply timelines, demand assumptions, and operational readiness with study teamsLead selection, oversight, and performance management of clinical packaging, labeling, depots, and distribution vendors; drive KPIs, quality, and continuous improvementOversee planning and execution of packaging and labeling campaigns, including master schedule development and issue resolution across stakeholdersSupport comparator sourcing, procurement, labeling, and distribution strategies, including coordination of complex global sourcing scenariosReview clinical protocols and develop fit-for-purpose clinical supply plans, including IRT considerations, aligned to study needs, timelines, and budgetPartner cross-functionally with Clinical Operations, Quality Assurance, Regulatory Affairs, CMC/Manufacturing, and Finance to ensure alignment, compliance, and timely decision-makingTranslate protocols and study assumptions into demand forecasts across scenarios; communicate risks, constraints, and recommendations to stakeholdersOversee clinical labeling strategy and execution (label design, translation oversight, production, change control) ensuring country and regulatory requirements are metDevelop and maintain integrated supply plans to support forecasts, including overage strategy, inventory governance, and regular updates to project teams and leadershipManage global distribution and logistics activities for assigned clinical studies, including import/export coordination, temperature-controlled shipments, and oversight of 3PL/regional depot partnersManage packaging/distribution scope and vendor coordination, including support for contracts, supply plan design, and development/approval of distribution instructions and operational playbooksOwn risk management for clinical supply (e.g., demand, lead times, quality, distribution), drive mitigation plans, and escalate critical issues with clear options and recommendationsSupport Interactive Response Technology (IRT) configuration and testing activities, including specification review, UAT coordination, and go-live readiness in partnership with Clinical Operations and vendorsOversee study closeout activities including drug reconciliation, returns/destruction strategy, and final inventory disposition in compliance with applicable requirementsEnsure clinical supply deliverables and documentation are inspection-ready and appropriately filed in the eTMF in alignment with Quality standardsDevelop, manage, and forecast clinical supply budgets for assigned studies/programs; track spend, purchase orders, and accruals; provide financial transparency to stakeholdersEstablish and monitor clinical supply timelines and key milestones; drive issue management, governance, and executive-ready communication for on-time deliveryStand-Out Skills for Impact:Strategic clinical supply planning mindset with the ability to translate protocol design, enrollment assumptions, manufacturing constraints, and country requirements into practical, risk-based supply strategiesStrong analytical capability to manage forecasts, inventory signals, resupply triggers, expiry exposure, and scenario planning across global studiesDemonstrated vendor management across packaging, labeling, depots, logistics providers, CMOs/CPOs, CROs, and IRT partners, including clear expectations, escalation pathways, and performance accountabilityOperational agility and sound judgment to anticipate supply disruptions, evaluate trade-offs, and drive timely decisions in a fast-paced clinical development environmentClear, executive-ready communication style with the ability to influence cross-functional stakeholders and communicate risks, options, and recommendations with confidenceQualifications:BS/BA degree required (advanced degree a plus) with 4+ years of progressive experience in Clinical Supply Chain within a biotechnology or pharmaceutical environment, including study-level ownershipDemonstrated experience leading contract packaging and labeling organizations, including governance, performance management, and issue escalationProven ability to develop and execute risk-based supply plans across early- to late-stage clinical development studies, including scenario planning and trade-off decision supportStrong understanding of global regulatory expectations for clinical supply distribution across US, EU, and APAC, including testing, labeling, and import/export requirementsDeep knowledge of cGMP, GCP, GDP, and transportation requirements for pharmaceutical materials; experience supporting inspection readiness and deviation/CAPA investigations as applicableExtensive global distribution experience, including regional depot strategy and operational execution; familiarity partnering with QP release processes and IRT providersStrong project management skills with demonstrated ability to coordinate cross-functional teams, influence without authority, and communicate effectively with internal and external stakeholdersThrives in a fast-paced innovative environment while remaining flexible, proactive, resourceful, and efficient; demonstrated ability to support scalable processes and train othersExperience using IRT/IXRS, inventory tracking tools, vendor portals, ERP modules, Smartsheet, Excel, or similar systems to manage clinical supply inventory, shipments, forecasts, and documentationDemonstrated ability to manage temperature-controlled clinical supply operations, including excursion review, documentation, mitigation planning, and coordination with Quality and logistics partnersExperience supporting clinical supply documentation such as label text, packaging records, distribution instructions, shipping documentation, inventory reconciliations, and study closeout recordsAbility to balance patient supply continuity, cost discipline, expiry/scrap risk, and operational feasibility when developing clinical supply recommendationsCompensation decisions are based on objective criteria including role responsibilities, experience/qualifications, internal equity, geographic location, and external market benchmarks.Pay Range$160,000—$170,000 USDKiniksa is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, transgender status, age, genetics, national origin, protected veteran status, or disability status, or any other legally protected category. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Kiniksa does not accept unsolicited resumes from staffing agencies or search firms. Any resumes submitted without a signed agreement will be considered property of Kiniksa, and no fees will be paid.