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 globally
• Ensure on-time startup and ongoing execution of new studies by aligning supply timelines, demand assumptions, and operational readiness with study teams
• Lead selection, oversight, and performance management of clinical packaging, labeling, depots, and distribution vendors; drive KPIs, quality, and continuous improvement
• Oversee planning and execution of packaging and labeling campaigns, including master schedule development and issue resolution across stakeholders

• Support comparator sourcing, procurement, labeling, and distribution strategies, including coordination of complex global sourcing scenarios
• Review clinical protocols and develop fit-for-purpose clinical supply plans, including IRT considerations, aligned to study needs, timelines, and budget

• Partner cross-functionally with Clinical Operations, Quality Assurance, Regulatory Affairs, CMC/Manufacturing, and Finance to ensure alignment, compliance, and timely decision-making
• Translate protocols and study assumptions into demand forecasts across scenarios; communicate risks, constraints, and recommendations to stakeholders
• Oversee clinical labeling strategy and execution (label design, translation oversight, production, change control) ensuring country and regulatory requirements are met
• Develop and maintain integrated supply plans to support forecasts, including overage strategy, inventory governance, and regular updates to project teams and leadership

• Manage global distribution and logistics activities for assigned clinical studies, including import/export coordination, temperature-controlled shipments, and oversight of 3PL/regional depot partners
• Manage packaging/distribution scope and vendor coordination, including support for contracts, supply plan design, and development/approval of distribution instructions and operational playbooks

• Own risk management for clinical supply (e.g., demand, lead times, quality, distribution), drive mitigation plans, and escalate critical issues with clear options and recommendations

• Support Interactive Response Technology (IRT) configuration and testing activities, including specification review, UAT coordination, and go-live readiness in partnership with Clinical Operations and vendors

• Oversee study closeout activities including drug reconciliation, returns/destruction strategy, and final inventory disposition in compliance with applicable requirements
• Ensure clinical supply deliverables and documentation are inspection-ready and appropriately filed in the eTMF in alignment with Quality standards
• Develop, manage, and forecast clinical supply budgets for assigned studies/programs; track spend, purchase orders, and accruals; provide financial transparency to stakeholders
• Establish and monitor clinical supply timelines and key milestones; drive issue management, governance, and executive-ready communication for on-time delivery

Stand-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 strategies
• Strong analytical capability to manage forecasts, inventory signals, resupply triggers, expiry exposure, and scenario planning across global studies
• Demonstrated vendor management across packaging, labeling, depots, logistics providers, CMOs/CPOs, CROs, and IRT partners, including clear expectations, escalation pathways, and performance accountability
• Operational agility and sound judgment to anticipate supply disruptions, evaluate trade-offs, and drive timely decisions in a fast-paced clinical development environment
• Clear, executive-ready communication style with the ability to influence cross-functional stakeholders and communicate risks, options, and recommendations with confidence

Qualifications:

• 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 ownership

• Demonstrated experience leading contract packaging and labeling organizations, including governance, performance management, and issue escalation

• Proven ability to develop and execute risk-based supply plans across early- to late-stage clinical development studies, including scenario planning and trade-off decision support

• Strong understanding of global regulatory expectations for clinical supply distribution across US, EU, and APAC, including testing, labeling, and import/export requirements
• Deep knowledge of cGMP, GCP, GDP, and transportation requirements for pharmaceutical materials; experience supporting inspection readiness and deviation/CAPA investigations as applicable
• Extensive global distribution experience, including regional depot strategy and operational execution; familiarity partnering with QP release processes and IRT providers

• Strong project management skills with demonstrated ability to coordinate cross-functional teams, influence without authority, and communicate effectively with internal and external stakeholders
• Thrives in a fast-paced innovative environment while remaining flexible, proactive, resourceful, and efficient; demonstrated ability to support scalable processes and train others
• Experience using IRT/IXRS, inventory tracking tools, vendor portals, ERP modules, Smartsheet, Excel, or similar systems to manage clinical supply inventory, shipments, forecasts, and documentation
• Demonstrated ability to manage temperature-controlled clinical supply operations, including excursion review, documentation, mitigation planning, and coordination with Quality and logistics partners
• Experience supporting clinical supply documentation such as label text, packaging records, distribution instructions, shipping documentation, inventory reconciliations, and study closeout records
• Ability to balance patient supply continuity, cost discipline, expiry/scrap risk, and operational feasibility when developing clinical supply recommendations

Compensation decisions are based on objective criteria including role responsibilities, experience/qualifications, internal equity, geographic location, and external market benchmarks.

Kiniksa 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.