• Lead the full lifecycle development of healthcare nutrition products, including thickened liquids, texture-modified foods, oral nutritional supplements, and hydration solutions for dysphagia patients. • Ensure all products meet clinical requirements for safety, efficacy, palatability, and compliance with IDDSI standards. • Drive formulation strategies that balance nutritional adequacy, sensory acceptance, stability, and ease of use in clinical and homecare settings. • Collaborate with Operations and Quality to ensure scalable, compliant manufacturing processes. • Build a robust innovation pipeline addressing unmet needs in dysphagia, malnutrition, and related conditions.

• Identify operational needs for upcoming projects, track and review current assignments for CAT Operations staff • Resource CAT study projects as Resource Manager • Engage as Subject Matter Expert (SME) for CAT Operations activities • Provide operational oversight for designated CAT study projects • Engage in and coordinate resourcing activities for all CAT awarded projects • Identify training and skills gaps among staff; coordinate and assist with learning opportunities to enhance operations staff knowledge and skills of industry related regulations, processes, materials, and guidelines • Actively identify and engage in process improvement activities • Participate in QMD reviews and new QMD development • Author, collaborate, and review QMD documents and guidance documents • Coordinate and manage CAT Operations team meetings • Active engagement and oversight of study risk assessments, as they relate to operational activities • Work with department leaders to ensure alignment among CAT operational and clinical services • Lead and/or contribute to departmental initiatives that aim to implement policies, methods, techniques to contribute to existing service areas and department growth • Accountable for oversight of CAT study deliverables from Launch process to study close out • Assist and collaborate with Operations staff, Project Management, Contracts on vendor and study budget development, scope of work revisions, tracking and compliance • Assist in vendor management related concerns, including involvement with escalations, Vendor Management and Quality Assurance meetings • Review and assess ongoing budget utilization and revenue recognition with Operations Managers to ensure projects are meeting financial targets • Manage internal CAT operations meetings and other trial-specific meetings, as appropriate • Significant contributor to multiple strategic departmental, sponsor-related and cross-functional initiatives • Participate in business development activities including; but not limited to proposals input, capabilities, and bid defense meetings • Apply thorough knowledge of industry regulations and guidelines to ensure operational compliance during clinical trial conduct

• Supports Neurelis’ Medical Information function by leading the development and maintenance of core medical content • Provides product and disease-state training to internal stakeholders and vendors • Serves as a subject matter expert for internal and external audiences • Reviews and approves medical materials that are scientifically accurate and clinically relevant through the Medical/Legal/Regulatory (MLR) compliance process • Supports Publication Response Team activities and provides scientific presentations and evidence-based responses to payors in support of Market Access • Contributes to cross-functional Medical Affairs initiatives • Applies scientific expertise to address escalated product and disease-state inquiries • Develops quarterly internal newsletters • Maintains AMCP dossier updates and provides scientific input on company products • Supports vendor training activities and contributes to the oversight of Medical Information quality and operational performance.

• Provide strategic and scientific medical leadership for immunology product(s) • Become a disease state and product expert, providing feedback and insights to medical affairs deliverables, and cross-functional partners, including the design and implementation of Medical Affairs plans • Work closely with the medical field team to develop/enhance KOL and key institution engagement plans and participate in KOL engagement and development, establishing Sobi Inc as a scientific partner of choice • Help plan and execute advisory boards to obtain advice • Create a medical education strategy and drive tactics to increase product and disease state education (webinars, medical roundtables, symposium, congress presence, CME strategy) • Partner with the field medical team to identify key resource needs and to collaborate on developing field materials and tactics • Additionally, partner with the team to establish a medical training plan and provide training/education to cross-functional partners • Develop US immunology product(s) evidence generation strategy to address stakeholder (HCPs, payers, and patients) needs (including product differentiation, health outcomes), collaborating with HEOR and global partners • Oversee any medical affairs-led research initiatives, including US Phase IV clinical programs, post hoc analyses, and natural history studies, to address US needs • Additionally, the Senior Medical Director will be a key contributor to the global life cycle management-led activities, including programs for future indications, cytokine testing, Investigator-Initiated Study strategy, and overall input into the creation and execution of product evidence generation plans • Oversee the US products publication strategy and execution, as well as contribute to the global publication plan and publications • Partner with scientific communications to ensure timely dissemination of key scientific data and its incorporation into field materials and other educational resources • Design and implement a medical advisory plan, collate medical insights, partner with the field team, and share them internally • Analyze insights for adjustment to strategy and tactics • Develop and foster strong collaborative relationships with internal partners, including Regulatory Affairs, Clinical Operations, Market Access, Medical Information, Pharmacovigilance, Sales and Marketing, Global product leadership, Global medical affairs, and clinical development, providing strategic medical insight and product/disease-state expertise to meet business objectives • Support the market access team as needed with medical expertise and in discussions/presentations to payers • Collaborate closely with global medical and clinical colleagues, ensuring US perspective and insights are incorporated into global initiatives • Interact with Key Opinion Leaders, Regulatory Authorities, Patient advocacy groups, and other external agencies in support of our products/ therapeutic areas of interest to advance company objectives to improve patient outcomes • Lead, or help lead, US product medical activities, including the US brand medical team.