Clinical Supply Specialist II - Onsite in Aliso Viejo, CA

How You’ll Contribute: The Clinical Supply Specialist II is responsible for supporting the planning, coordination, and execution of clinical supply activities across assigned clinical programs. This role applies working knowledge of clinical supply chain processes to ensure investigational product is available to clinical sites in accordance with study timelines, regulatory requirements, and quality standards. The position contributes to forecasting, distribution planning, and vendor coordination while collaborating with internal stakeholders and external partners. The Clinical Supply Specialist II operates with moderate independence, solving a range of defined problems and supporting continuous improvement in supply chain processes. What You’ll Do: This role supports the execution of clinical supply strategies and operational activities for assigned studies, ensuring timely delivery and compliance with applicable standards. The position collaborates cross-functionally and contributes to effective supply planning and issue resolution. * Support development and execution of clinical supply plans, including forecasting, distribution, and inventory management for assigned studies * Coordinate investigational product shipments to clinical sites, ensuring compliance with regulatory, quality, and study requirements * Collaborate with Clinical Operations, CMC, Manufacturing, Quality, and external vendors to ensure supply readiness and continuity * Monitor inventory levels and study demand, identifying potential risks and escalating issues as needed * Assist in packaging, labeling, and distribution activities, ensuring alignment with protocol requirements and regulatory standards (e.g., GCP,

FDA)

* Maintain accurate supply documentation, tracking systems, and study records to ensure audit readiness * Contribute to vendor coordination activities, including communication, performance tracking, and issue resolution * Support implementation of supply chain processes, tools, and best practices to improve efficiency and reliability * Participate in study team meetings to provide updates on supply status, risks, and mitigation plans How You’ll Get There: * Typically requires 2–5 years of experience in clinical supply chain, clinical operations or related field * Experience supporting clinical trials or regulated environments, including investigational product handling and distribution * Working knowledge of clinical supply processes, including forecasting, inventory tracking, and logistics coordination * Ability to analyze data and resolve moderately complex issues using established procedures and practices * Experience collaborating across functions and building effective working relationships with internal and external stakeholders

• Strong organizational, communication, and project coordination skills
• Experience with clinical supply systems (e.g., IRT or inventory systems)

preferred * Bachelor’s degree required (biological sciences, health sciences, supply chain, engineering, business, or related discipline).

• 81,000.00 - 101,200.00 Range plus full benefits package
• This role works onsite in our worldwide headquarters, Aliso Viejo, CA

#GKOSUS

Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases. Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases. Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients. Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra “We’ll Go First,” which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do. Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol “GKOS”. Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts. Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. All offers of employment are contingent upon the successful completion of a background check, including successfully passing a drug screen, based on the position and local regulations.