• Build the clinical architecture for proactive, longevity-focused care delivery • Design assessment frameworks, biomarker panels, and care pathways • Establish the clinical standards that differentiate Anomaly's model from both traditional medicine and wellness noise • Shape how we use technology, AI, and async care to deliver at scale without compromising quality • Be the clinical voice in product, strategy, and client relationships

• Act as the lead clinical liaison for partner providers, representing Cadence across multiple regions • Partner with PRMs on clinic visits, field travel, and ongoing relationship management • Explain and advocate for the clinical value of our care models; address provider questions on services, data, and protocols • Support onboarding and training for new clinics, ensuring clinical confidence and alignment • Resolve provider complaints with empathy and follow-through • Surface field insights to internal teams (clinical, product, engineering) to guide service improvements • Stay current on RPM, CCM, APCM, and regulatory standards to ensure compliant, high-quality care

• Support development and execution of the United States Medical Affairs strategy for encaleret in ADH1 and chronic hypoparathyroidism, including launch readiness and lifecycle planning with scientific rigor and patient focused decision making • Support integrated evidence generation planning and execution, including real world evidence, Phase 4 studies, registries, investigator-initiated research support, and data integration activities • Support omnichannel HCP engagement by enabling field and digital scientific exchange, gathering insights, and translating themes into Medical Affairs programs and tactics • Support strategic relationships with key opinion leaders, investigators, and external stakeholders across endocrinology, nephrology, and related specialties, and co-lead advisory boards and expert panels • Partner with Clinical Development to support ongoing and planned clinical trials and contribute to data disclosure and publication planning with Scientific Communications • Support peer to peer scientific exchange and external education programs, including congress and clinical meeting preparation and scientific materials development • Partner with Congress Operations and Scientific Communications to define congress strategy, align scientific narratives and data priorities, and deliver coordinated pre congress, onsite, and post congress medical plans • Ability to travel up to ~40% for scientific meetings, advisory boards, and internal engagements

• Design, organize, lead and execute training sessions for care professionals on product knowledge effectively • Ensure patients globally in both clinical trial and commercial settings are treated at the highest standards and if necessary to provide onsite support • Plan, organize, and execute Investigator Meetings, Advisory Board Meetings and other equivalent events and present on behalf of the company as needed • Support research, development and commercialization efforts through collecting and synthesizing observation in the medical field and clinicians’ feedback • Develop robust partnership relationship with HCPs within current and future therapeutic area • Educating employees the insights and information gained from academic papers and conference • Identify challenges for the mid to long-term global R&D and medical communication and propose/execute solutions from medical perspective.