• Serve as the Lead Clinical Programmer on Pulmovant sponsored clinical trials, utilizing Veeva CDMS, Medidata RaveEDC, and/or InForm as the primary electronic data capture (EDC) solutions. • Perform hands-on design and build of Case Report Forms (CRFs), associated visit matrices, edit checks, rules and custom functions, or alternatively, oversee a Contract Research Organization (CRO) that performs these activities. • Select and maintain clinical data tools, including performing product validation for the organization. • Integrate multiple other critical clinical data products into EDC (e.g., Interactive Response Technology, electronic Patient Reported Outcomes, etc.) via API or other methods. • Lead User Acceptance Testing (UAT) process for a cross-functional team, including authoring UAT plans and other required validation documentation. • Participate in protocol review and study design discussion as subject matter expert on CDISC/CDASH best practices. • Work closely with the Head of Clinical Data Management and other Biometrics leaders to build and maintain a growing global library of SDTM/CDASH compliant CRFs, edit checks, and downstream reports, listings, and visualizations. • Perform and validate data migrations and/or post-production database changes needed after initial database go-live. • Program project-specific metrics reporting, working across the project team to ensure reports meet the needs of all internal and external stakeholders. • Author and maintain appropriate Standard Operating Procedures (SOPs) that govern the database build, handling, transfer, and cleaning processes. • Oversee clinical database build timelines, in concert with the Lead Clinical Data Manager, Project Manager, and other critical study team members. • Author and maintain Data Transfer Agreements with external vendors, in addition to being point of contact for any incoming or outgoing clinical data transfers via a secure method. • Heavily support data management activities, including data review and cleaning, query resolution, data reconciliation, authoring Data Management documentation, and coordination of database freeze/lock deliverable. • Train internal and external stakeholders on clinical database functionality as needed. • Perform and own the user management process at a study-level. • Primary point of contact for organization as business owner of multiple vendors, including notably the clinical database vendors. • Oversee and drive vendor governance in this capacity. • Own clinical data aggregation process and select appropriate technology tools to enable this (e.g., Veeva CDB).

• Draft, revise, and edit scientific publications, including manuscripts for peer-reviewed journals as well as abstracts, posters, and oral presentations for medical conferences. • Collaborate with Publication Planning team to coordinate kick-off calls with Investigators and establish timelines for the development of publications. • Work with internal stakeholders to ensure publications are clear, accurate, and aligned with strategic goals. • Participate in meetings with clinical trial investigators and key opinion leaders for the review and revision of drafts and to manage the editing and revision process, ensuring timely completion of scientific publications. • Keep current with the latest information, trends, and developments in target therapy areas, and perform literature searches as needed for drafting publications. Interpret literature information relevant to scientific publications. Understand, assimilate, and interpret data and other sources of information with appropriate guidance/direction from authors and therapeutic teams. • Remain current on industry and company requirements and best practices as they relate to scientific publications. • Understand and follow applicable company publication policy and procedures and act as a subject matter expert regarding internal processes and relevant publication guidelines.

• Serve as the medical content lead for a Therapeutic Area • Interface with key stakeholders across CMR, Marketing, and the Global organization to support strategic development and execution • Lead the Core Medical Team, Project Team, and National Advisory Board meetings • Represent NNI on Global Project Teams (GPT) and Commercial Access Teams (CAT) • Provide detailed medical evaluation of assets under consideration for licensing and/or acquisition • Gain endorsement of Medical Product Plan from Medical Affairs and overall CMR management • Align Medical Product Plan with Commercial colleagues • Partner with Project Manager to track key projects in Medical Product Plan and report on budget status • Lead planning and execution of National Advisory Board meetings • Develop trusting working relationships with Project Vice Presidents (PVP) relevant for therapeutic area • Present findings and recommendations to NNI management

• Define and own Hone’s longevity medicine strategy, including our clinical protocols, therapeutic frameworks, and evidence standards • Serve as the primary scientific voice for Hone’s approach to hormone optimization, metabolic health, gut health, immunity, cardiac care, and other longevity-focused therapeutic areas • Stay at the forefront of longevity science and translate emerging research into actionable clinical insights and product improvements • Oversee the development and continuous improvement of clinical protocols in partnership with Hone-affiliated medical practices • Oversee the integration of clinical protocols into the 'Longevity Operating System,' which is Hone's proprietary AI tech to drive the clinical decisions to support Patient care • Champion patient outcomes by establishing clinical quality benchmarks and driving continuous improvement across the care model • Collaborate with Care Team leadership to ensure patient-facing interactions are grounded in empathy, accuracy, and clinical integrity • Identify gaps in the patient journey that represent opportunities to improve health outcomes or patient satisfaction • Serve as a member of Hone’s executive leadership team, contributing to company strategy, culture, and decision-making • Serve as a thought leader and spokesperson for Hone externally, including media, conferences, and strategic partnerships • Build and mentor a team of clinical and scientific advisors as the function scales • Model Hone’s values and people-first culture in all interactions