• Develop and implement the strategic roadmap for outpatient therapy program across all senior living sites, identifying short- and long-term goals with defined milestones and phased implementation plans. • Design and standardize therapy program models, clinical workflows, documentation standards and performance frameworks – ensuring consistency and scalability across all sites. • Own end-to-end site operations from pre-launch, site assessment, equipment procurement approval, through collaborating with local branch clinical and operational leadership for staffing, scheduling, and care delivery. • Establish evidence-based clinical protocols for the geriatric outpatient population across fall prevention, functional rehabilitation, chronic disease management, and post-acute recovery. • Monitor and report clinical and operational KPIs including units per clinician, hospitalization avoidance, plan of care goal achievement, and ADC and revenue per community – with regular executive-level reporting to leadership. • Partners with Strategic Business Development, Sales Leaders, and Senior Living Partnership Executives to ensure program delivery actively supports and protects preferred provider partnerships. • Lead routine partnership reviews with senior living operators, presenting outcomes data, operational performance, and forward-looking program recommendations that reinforce the preferred provider relationship. • Serve as a senior-level clinical presence and brand ambassador within the senior living portfolio, ensuring every clinical touchpoint reflects the service excellence standards that differentiate the program competitively.

• design, operationalize, and scale the Customer Success (CS) model for Huron’s Healthcare Insights portfolio • establish a cohesive, enterprise-ready CS framework that can be extended across adjacent products • define and operationalize a coordinated service structure, including: Base SaaS offerings (self-service model), Managed services, Buy-up / enhancement services • build, lead, and develop a high-performing CS Insights program • own and mature the Engagement Health program for monitoring and improving client outcomes • establish and scale a formal account management capability across Insights products • define the end-to-end customer lifecycle model • support the broader vision of a unified Healthcare Insights platform

• Define and execute the overall clinical quality strategy and direction of the organization • Lead the design and execution of all clinical training and quality oversight for data abstraction • Serve as subject matter expert for risk-adjustment and HEDIS • Responsible for training all internal staff, partners, and vendors internationally • Responsible for execution of all Joint Quality Audit processes • Collaborate with Innovation team for new market capabilities • Maintain compliance with Inovalon's policies, procedures, and mission statement

• In collaboration with the Head of Clinical Development, provide strategic and medical leadership for the bezuclastinib clinical development program in GIST • Provide clinical and medical support to life cycle management activities in GIST as needed • Collaborate with commercial and medical affairs colleagues to support launch activities for bezuclastinib in GIST • Provide primary medical monitor responsibilities, including oversight of trial subject safety and clinical data review and interpretation for the Peak clinical trial • Design, prepare and initiate study protocols and other required documentation in compliance with project plans, federal regulations, good clinical practice (GCP) and good medical practice • Work collaboratively with matrix team members in trial execution and oversight • Provide support to the clinical trial study team to manage safety, site education, protocol-related and eligibility questions • Provide medical oversight and input into clinical trial documents including but not limited to the study protocol, informed consent form (ICF), statistical analysis plan (SAP), case report form (CRF), clinical study report (CSR) • Provide medical and scientific input into other documents including but not limited to the investigators’ brochure, regulatory filings and submissions, abstracts, manuscripts and publications, clinical study reports • Collaborate with the regulatory team to develop briefing documents and other regulatory documents in support of submissions • Interact with clinical trial sites, external clinical experts, contract research organizations (CROs) and regulatory agencies • Support investigator meetings, steering committee meetings, data monitoring committee reviews as the study physician • Assist with regulatory submissions by answering protocol-related questions from regulatory authorities, ethics committees and institutional review boards (IRBs) • Develop a deep understanding of the clinical and competitive environment and work with the asset team to develop the target product profile