• Assist the Chief Medical Director to direct and coordinate the medical management, quality improvement and credentialing functions for the business unit. • Provides medical leadership of all for utilization management, cost containment, and medical quality improvement activities. • Performs medical review activities pertaining to utilization review, quality assurance, and medical review of complex, controversial, or experimental medical services, ensuring timely and quality decision making. • Supports effective implementation of performance improvement initiatives for capitated providers. • Assists Chief Medical Director in planning and establishing goals and policies to improve quality and cost-effectiveness of care and service for members. • Provides medical expertise in the operation of approved quality improvement and utilization management programs in accordance with regulatory, state, corporate, and accreditation requirements. • Assists the Chief Medical Director in the functioning of the physician committees including committee structure, processes, and membership. • Conduct regular rounds to assess and coordinate care for high-risk patients, collaborating with care management teams to optimize outcomes. • Collaborates effectively with clinical teams, network providers, appeals team, medical and pharmacy consultants for reviewing complex cases and medical necessity appeals. • Participates in provider network development and new market expansion as appropriate. • Assists in the development and implementation of physician education with respect to clinical issues and policies. • Identifies utilization review studies and evaluates adverse trends in utilization of medical services, unusual provider practice patterns, and adequacy of benefit/payment components. • Identifies clinical quality improvement studies to assist in reducing unwarranted variation in clinical practice in order to improve the quality and cost of care. • Interfaces with physicians and other providers in order to facilitate implementation of recommendations to providers that would improve utilization and health care quality. • Reviews claims involving complex, controversial, or unusual or new services in order to determine medical necessity and appropriate payment. • Develops alliances with the provider community through the development and implementation of the medical management programs. • May represent the business unit before various publics both locally and nationally on medical philosophy, policies, and related issues. • Represents the business unit at appropriate state committees and other ad hoc committees. • May be required to work weekends and holidays in support of business operations, as needed.

Role Description The Medical Science Director will serve as an internal scientific expert supporting products in an assigned therapeutic area. This role has responsibility for responding to Medical Information Requests, clinical support for the field sales teams, clinical support for customers, and the product development strategy. - Provide clinical and scientific expertise in the assigned therapeutic area to support internal teams, healthcare professionals (HCPs), and stakeholders. - Respond to medical information requests from healthcare providers, external partners, and internal departments with accurate, balanced, and timely information. - Lead and participate in advisory boards, KOL engagements, and scientific exchange to gather and provide insights for product development and medical strategy. - Collaborate with Clinical Operations to provide medical oversight and support for clinical trials including investigator-initiated studies. - Work closely with cross-functional teams (R&D, clinical development, regulatory affairs, commercial) to ensure medical insights are integrated into company strategies and product life cycle management. - Develop and deliver high-quality scientific presentations and materials for both internal and external audiences, including HCPs and key opinion leaders (KOLs). - Ensure that all medical communication, promotional material reviews, and activities comply with regulatory requirements, company policies, and ethical standards. - Provide ongoing medical and scientific training to internal teams, including sales and medical affairs, to ensure a deep understanding of oncology products and disease states. Company Description

• responsible for assigned aspects of medical policies and programs • performs medical reviews • interacts with the provider communities for assigned areas

• 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.