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

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