• Act as the primary builder and subject matter expert designing our upcoming longitudinal Serious Mental Illness (SMI) care model • Design clinical strategies optimized for Total Cost of Care (TCOC) reduction and ED diversion • Partner directly with our clinical operations and engineering teams to continuously build and optimize our proprietary EMR, integrating generative AI tools • Define and track the program’s ultimate scorecard utilizing advanced, population-health KPIs • Act as the primary, hands-on treating psychiatrist and prescriber for our most complex, medically fragile geriatric members • Direct structured, data-informed case reviews with your panel of behavioral health care managers • Scale our internal asynchronous psychiatry e-consult program • Work closely with the BH social work manager to provide clinical oversight and serve as the key clinical escalation point for the behavioral health team

Role Description Genmab is currently seeking a Hematology Medical Science Liaison (MSL)/Senior MSL (Sr. MSL) to be a part of an exciting opportunity of a passionate, high profile, high-impact Global Medical Affairs team, and work in a dynamic and collaborative setting. The MSL/Sr. MSL is a member of a field-based team of advanced degree specialists who function as an extension of the Global Medical Affairs organization. MSLs are responsible for developing and enhancing professional relationships with medical thought leaders to support both Genmab approved products and those in various phases of development. MSLs provide medical information through scientific exchange in a fair and balanced manner and provide clinical/scientific support for Genmab’s pipeline. Domestic travel of approximately 50% will be required. Territory will be GA, AR, MS, LA, AL. Responsibilities will include, but are not limited to, the following: - Identify key thought leaders and establish, foster, cultivate, and maintain relationships with healthcare providers (HCPs) in academic and community centers within assigned territory. - Develop and execute territory plans in alignment with regional, national, and global Medical Affairs strategies. - Provide insights/feedback on emerging scientific/clinical data that enhance the value and appropriate use of Genmab products as part of compliant collaboration with internal stakeholders. - Present appropriate clinical and scientific information to healthcare providers in response to unsolicited requests (as appropriate) in a fair and balanced manner. - Provide medical and scientific education relative to disease state and Genmab products to healthcare providers. - Support product launches through HCP education for safe use of our medicines. - Act as the primary point of contact and facilitator for all aspects of investigator sponsored trials (ISTs), from submission, review and approval, through study activation/completion. - Collaborate effectively and proactively establish working relationships with cross-functional teams. - In collaboration with medical and clinical operations teams, support Genmab-sponsored trials through trial site recommendations and raising awareness of the trials and accrual timelines. - Maintain up-to-date knowledge of products, clinical treatment trends, clinical trials, and scientific activities within areas of interest to Genmab ie: oncology and hematology. - Serve as scientific resource to commercial partners, as appropriate, to support activities. - Support the execution, organization, and planning of advisory boards. - Professionally represent Genmab at select medical and scientific conferences and meetings. Qualifications - Advanced/scientific medical degree strongly preferred (PharmD, PhD, MD). Candidates with a clinical background (e.g., NP, PA, etc.) and extensive hematology/oncology experience will be considered. - At least 2 years MSL/Medical Affairs experience in Oncology/Hematology focus preferred. - Strong knowledge and/or experience of healthcare and access environments. - Proven ability to work independently, as well as cross-functionally with numerous internal stakeholders in a high-matrixed environment, including joint venture collaborations. - Preferred experience on product launches or demonstrated success as product or therapeutic point. - Excellent interpersonal communication and presentation skills, strong personal integrity, teamwork abilities, and a customer focus are necessary. - Must be able to organize, prioritize, and work effectively in a constantly changing environment. - Strong compliance knowledge and adherence to corporate compliance policies. - Current working knowledge of FDA, OIG, ICH, GCP, PhRMA Code, HIPAA and other compliance regulations and guidelines relevant to industry interactions with healthcare professionals. - Demonstrated technical acumen including MS Office skills, ability to adopt and leverage multiple business applications. Requirements For US based candidates, the proposed salary band for this position is as follows: - $162,320.00---$243,480.00 The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives. Benefits - 401(k) Plan: 100% match on the first 6% of contributions. - Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance. - Voluntary Plans: Critical illness, accident, and hospital indemnity insurance. - Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave. - Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support. - Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses.

Role Description We are looking for a Medical Affairs Lead, who is responsible for shaping and delivering the DACH medical strategy, driving education, evidence generation, and engagement with healthcare professionals and key opinion leaders in the diabetes space. The role leads cross-functional collaboration to support product launches, market access, and adoption of Insulet’s solutions. The Medical Affairs Lead for DACH is accountable for developing and executing the Medical Affairs strategy for the 3 countries. They lead the creation and execution of the country medical plans in alignment with the business objectives of the Insulet’s affiliate. The medical plans encompass value-generating activities on: - Medical education - Evidence generation and dissemination - HCP and KOL engagement - Internal knowledge and insights translation This individual has leadership responsibilities to ensure the execution of all above tasks. They will be responsible to lead a team in the development and successful execution of medical strategies and tactics that enhance regulatory approval, customer access, and adoption of Omnipod products in the region. Responsibilities - Supervise country Medical Affairs staff focused on delivering the medical objectives for the region by providing direction, guidance, and oversight of assigned projects and accountabilities. - Develop and lead the execution of the Medical Affairs strategy at a country level through cross-functional collaboration and influence – supporting efficient go-to-market plans. - Lead, establish and execute the local medical education plans for the DACH: educate HCP with online/in-person blended offerings (on-demand, webinars, Peer-to-Peer training), deliver medical education at congresses and symposiums, support product training with generation and delivery of medical content. - Inform & strategize evidence generation plans, in answer to fulfill market access, regulatory, and marketing needs. - Support the local execution of Insulet-sponsored and Investigator-Initiated trials. - Disseminate evidence. - Identify and engage with HCP to inform and seek advice on the company’s solutions, through the execution of advisory boards, clinical activity, scientific exchange, and educational events. - Establish and maintain credible peer-to-peer scientific relationships with national and regional KOLs. - Build confidence and advocacy among key external influencers (KOLs). - Build and share knowledge with internal and external stakeholders regarding the use and benefits of current and future Insulet products. - Work collaboratively with cross-functional partners. - Translate clinical data into scientifically sound, tangible insights and claims. - Review and approve externally-facing materials for scientific and medical accuracy. - Review scientific and medical content for externally-facing content, using the Veeva system. - Answer HCP medical queries. - Assist with sales events such as pump clinics, pump support groups, info sessions, in-the-office educational events, patient info nights, advocacy events, etc. - Maintain a thorough and detailed working knowledge of the organization and its products, current scientific research, and publications. - Perform other duties as required. Key Decision Rights - Country Medical strategy, including launch plans. - KOL engagement activity. - Medical Education activities for the DACH. Qualifications - MD, PharmD, PhD or MS in life science or an equivalent. - 8 or more years of relevant or equivalent Medical Affairs experience in diabetes within the pharmaceutical or medical device industry. - In-depth understanding of the diabetes disease state, the current/future treatment landscape, and ongoing clinical trials/research. - Understanding of the country medical practice and clinical decision-making regarding patient care for diabetes. Skills/Competencies - Proven leader in Medical Affairs including developing and leading the implementation of medical strategy. - Excellent written and verbal communication skills in English. - Broad understanding of the international commercial and regulatory environment for medical devices. - Strong scientific acumen and attention to detail. - Combined strategic thinking and execution skills. - Demonstrated ability to integrate, lead and influence in a challenging cross-functional environment. - High ethical standards which apply to interactions with HCPs, payers, and industry representatives. Physical Requirements - Location: Germany - This role will involve frequent travel, approximately 40% mainly in the DACH region and within the international region on occasions (conferences, medical education events, internal meetings). Company Description Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. For more information, please visit insulet.com and omnipod.com.

Role Description The Medical Benefit Underwriting Coordinator is responsible for assisting and supporting benefit underwriters with quoting, rating and issuance of new business quotes, renewals, and endorsements. This position also responds to problem situations from brokers and performs customer service tasks as needed. Job Responsibilities: - Review of incoming submissions and subsequent documents/reports for completeness along with class of policy (Group or Individual), branch code and other required information. - Work with Underwriters and Sales staff to assess submitted information. - Process reserves in policy issuance system. - Participate as needed in systems and workflow development as required. - Review workload daily to prioritize timelines for medical underwriting review submissions. - Work with management as issues arise. - Support our Benefits Underwriting Department with daily tasks. - Assist underwriters in managing a book of business and help improve the underwriting process. - Assist the Claims Department with authorized services, narratives, and reserves. Qualifications - Any level of nursing: LPN/RN/BSN/MSN. - 3 years or more with experience in risk, finance, utilization and/or case management. - Health Insurance Underwriting experience is a plus. - Willingness to learn and develop strong technical skills in Health Insurance Industry. - Comprehension of claims review and analytics desirable. - Stoploss/Reinsurance or payor experience a plus. Requirements - Nursing: LPN, RN, BSN, CM or other related certifications a plus. Benefits - Paid time off for company holidays, vacation, sick and personal days. - Paid parental leave. - Mental health services. - Comprehensive and best-in-class benefits package. Company Description Ryan Specialty is an Equal Opportunity Employer. We are committed to building and sustaining a diverse workforce throughout the organization. Our vision is an inclusive and equitable workplace where all employees are valued for and evaluated on their performance and contributions. Differences in race, creed, color, religious beliefs, physical or mental capabilities, gender identity or expression, sexual orientation, and many other characteristics bring together varied perspectives and add value to the service we provide our clients, trading partners, and communities.