• 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.

Role Description The Medical Director participates in the broad array of activities of the Medical Services area including, but not limited to: - Medical and Pharmacy Utilization Management - Quality management - Member care management - Medical policy processes - Support for various lines of business The incumbent also provides input into the development of policies, programs, and strategic objectives that cover Medical Management Services through their required participation in various committees and when assigned to other committees or workgroups as requested by leadership. They also act as a liaison with local physicians and hospitals and keep abreast of practice patterns, issues, and concerns of their regional medical community, as well as support our Provider Relations team as requested. This position is occasionally required to work evenings during high volume periods and staff shortages, e.g. cross-coverage vacations. Qualifications - Minimum of seven (7) years of clinical practice experience after completion of all graduate medical education training, including residency and fellowship (when applicable). - Medical Degree: MD or DO from an accredited institution required. - Active board certification in Professional Medical Specialty. - Active unrestricted medical license to practice medicine in a state or territory of the United States. - The Physician is not the subject of any pending professional disciplinary action that could result in the impairment of their ability to practice medicine. - Knowledge of applicable state and federal laws, NCQA standards, and Utilization Management. - Demonstration of effective use of word processing, spreadsheet, email. - Strong interpersonal skills essential for communication to staff at all levels of the organization. - Demonstration of strong and effective abilities in teamwork, negotiation, conflict management, decision-making, and problem-solving skills. - Ability to work within changing business environment and balance patient advocacy with business needs. - Successful ability to assess complex issues, to determine and implement solutions, and resolve problems. - Demonstrated sensitivity to culturally diverse situations, participants, and customers/members. Requirements - Leads, develops, directs, and implements clinical and non-clinical activities that impact health care quality cost and outcomes. - Identifies and develops opportunities for innovation to increase effectiveness and quality. - Serves as a mentor or coach to other Medical Directors and other colleagues in quality and performance improvement processes. - Conduct clinical appeal case reviews and may require peer-to-peer discussions with providers regarding UM case review determinations. - Provides input into the utilization management program policies and procedures. - Assists in many aspects of frontline UM during high peak activity or staff outages. Benefits - Compensation Range: $202,000.00 - $303,000.00 - Participation in group health and/or dental insurance - Retirement plan - Wellness program - Paid time away from work - Paid holidays Physical Requirements - Ability to work prolonged periods sitting at a workstation and working on a computer. - Ability to work while sitting and/or standing while at a workstation viewing a computer and using a keyboard, mouse and/or phone for three (3) or more hours at a time. - Typical office environment including fluorescent lighting. - Ability to work in a home office for continuous periods of time for business continuity. - Ability to travel across the Health Plan service region for meetings and/or trainings as needed. - Ability to lift, carry, push or pull 15 pounds or less. - Manual dexterity including fine finger motion required. - Repetitive motion required. - The ability to hear, understand and speak clearly while using a phone, with or without a headset.

Role Description The Senior Medical Director (Hematology/Oncology) is a strategic medical leader who provides scientific, clinical, and operational oversight across global clinical research programs. Acting as Medical Monitor, this role serves as the primary medical interface between IQVIA, sponsors, and investigative sites—ensuring high-quality, compliant, and efficient trial execution. - Provides hands-on medical oversight, guiding protocol interpretation, eligibility, compliance, and safety. - Includes medical data review and review of critical clinical data (e.g., alert laboratory results) and timely response to urgent medical queries to ensure patient safety and study continuity. Qualifications - MD from an accredited, internationally recognized medical school. - 5–7+ years of clinical experience as a licensed physician within the relevant specialty (Oncology, Hematology, Surgical Oncology, or Urology with oncologic focus). - Board certification or eligibility in the relevant therapeutic area strongly preferred. - Proven experience in clinical research (≥3 years) as a study physician/investigator or within Pharma, CRO, or Biotech environments. Requirements - Strong ability to collaborate effectively within multidisciplinary and matrixed global teams, driving alignment and consensus. - Demonstrated ability to work independently while managing multiple priorities in a dynamic environment. - Excellent organizational skills with the ability to manage complex projects with shifting timelines and requirements. - Exceptional communication and interpersonal skills, with the ability to translate complex medical concepts into clear, actionable insights. Benefits - The potential base pay range for this role, when annualized, is $186,300.00 - $519,000.00. - Actual base pay offered may vary based on job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). - Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.