N-Power Medicine, Inc.

• Own end-to-end recruiting for clinical, technical, and AI roles in a fast paced, high-growth environment • Develop and implement effective recruiting strategies to attract a diverse pool of qualified and capable talent for our teams • Manage the full cycle, from identifying and engaging potential candidates through various channels, to conducting interviews and extending offers • Work closely with hiring managers to deeply understand technical requirements of the role, the function, and how it fits into the organization • Proactively source and engage top-tier diverse talent in competitive markets • Build and manage strong candidate pipelines while delivering a standout candidate experience • Adapt and iterate recruiting strategies as the company scales • Perform additional duties and responsibilities as required

• Design, implement, interpret, report and publish the results of retrospective and prospective observational research studies for life sciences customers • Support the development of N-Power Medicine’s data platform and assets, including specification of data models and clinical nomenclature/coding requirements to efficiently harmonize real-world data with clinical trials data standards, such as Clinical Data -Interchange Standards Consortium (CDISC) • Contribute to developing N-Power Medicine’s real-world evidence generation platform, in alignment with the company’s by-protocol, prospective real-time data • Collaborate with internal partners (Clinical Science, Commercial, and Network Partners) to develop the company's strategic partnerships with life sciences • Collaborate with internal partners (Clinical Science, Commercial, and Network Partners) to develop the data requirements to support N-Power Medicine’s next-generation External Controls methodology and product offerings • Help translate the perspectives and requirements of FDA and regulatory agencies around external controls to inform N-Power Medicine's data capture/collection and platform requirements • Ask the right scientific questions, ideate and make recommendations on fit-for-purpose data and analytics solutions • Stay current with novel data analysis methods for observational data, in particular Causal Inference and its applications to clinical trials • Perform additional duties and responsibilities as required

• Build expert capabilities in prospective ECAs and hybrid controls combining retrospective and prospective real world-data with single arm and randomized controlled trials. • Provide expertise for developing statistical methodologies that mitigate selection, confounding, and measurement bias in external control and hybrid control studies. • Guide and mentor internal teams on novel methodologies, best statistical practices, and innovative clinical trial designs. • Collaborate with Clinical Science and Commercial teams for innovative clinical development projects. • Define data requirements and data collections processes to enable next generation ECAs. • Lead or support research study design and end-to-end delivery, including study scoping and development of study protocols. • Co-author communications of study results in peer-reviewed publications and presentations.

• Partner with Commercial leadership to support enterprise biopharma sales, particularly for External control arms, pragmatic studies, clinical trials screening and other data products. • Lead technical and scientific discovery and scoping with pharma partners, including: study design considerations, clinical trial protocol review, cohort feasibility and data coverage, analytical approaches. • Serve as a key technical voice in customer meetings, RFPs, and scientific discussions, mastering knowledge for each of NPM’s product lines. • Partnering with business development on end-to-end scoping of customer engagements, with primary responsibility of (1) technical / scientific scoping and information request documents or presentations, (2) proposal / statement of work generation and (3) assessing timelines, costs and resourcing considerations. • Translate customer requirements into clear internal specifications for product, data science, engineering, delivery / program management. • Act as the bridge between sales and delivery, ensuring clean, well-documented handoffs,, no loss of context or commitments, alignment on success criteria and milestones. • Partner with product leadership to provide market-driven feedback on product gaps and roadmap priorities and shape packaging of data products and ECA offerings. • Build repeatable pre-sales frameworks, playbooks, and templates to improve sales efficiency and reduce custom scoping overhead. • Contribute to GTM strategy, including: ideal customer profiles, use case definition, pricing and packaging inputs. • Partner with marketing and product to translate internal technical or scientific concepts / data into sales collateral. • Perform additional duties and responsibilities as required.

• Oversee the end-to-end implementation and execution of assigned oncology studies across multiple Network sites, ensuring compliance with study protocols, timelines, and regulatory requirements. • Act as a strategic liaison between pharma sponsors, contract research organizations (CROs), clinical sites, and internal teams to ensure alignment and execution of study objectives. • Proactively identify operational risks and implement creative, timely solutions (SOPs, tools, and best practices) to optimize clinical trial workflow, patient recruitment, and data quality. • Collaborate with regulatory, data, quality, and site teams to ensure compliance with applicable regulations and internal SOPs. • Monitor trial progress, identify bottlenecks, and proactively address identified operational challenges. • Review and provide input on essential study documents (e.g., protocols, informed consents, site training materials). • Oversee trial-specific training for internal stakeholders and site teams. • Responsible for operational input and oversight in designing, planning, initiating and completing clinical trials across assigned disease teams. • Lead clinical study and cross functional team to make key decisions related to strategy and issue resolution. • Participate in initiatives to establish best practices for optimizing patient enrollment in clinical trials. • Collaborate with stakeholders to develop and implement trial specific training programs. • Innovate and implement novel patient enrollment strategies to maximize clinical trial participation. • Identify and integrate new tools, workflows, and methodologies to improve protocol implementation and patient enrollment processes. • Perform additional duties and responsibilities as required.

• Virtually accompany the healthcare provider in all scheduled visits into patient examination rooms in order to assist the provider by developing draft clinical notes. • Serve as the Company’s trusted face to the clinical practice, providing clinical support while improving routine care data quality. • Assist with chart preparation aligning with the healthcare provider’s (HCP’s) needs and documenting what has occurred since last visit. • Identify missing information needed for clinical trial pre-screening and prompt provider for needed information. • Successfully utilize the EMR to document all clinic activity including any procedures and assessments performed by the physician, as well as patient orders including laboratory tests, radiology tests, medications, etc. • Ensure adherence to protocol requirements and data quality standards. • Remind provider of relevant recommended evaluations when appropriate, with documentation to support data integrity. • Review completed charts with the provider as appropriate. • Ensure quality and integrity of data capture, compliance and confidentiality with Company’s and site’s policies, standard operating procedures (SOPs), and Good Clinical Practice (GCP). • Additional duties and responsibilities as required.

• Assists with the build of the NPM clinical platform including variable sets, conditional logic, automated quality checks, and the flow of the application for data curation • Develops work instructions and data guides to support variable sets built for the NPM platform • Works with our team of data engineers, clinical subject matter experts and other staff to support development and implement quality data variables • Ensure adherence to the study protocols and data completeness • Work closely with the Operations and Quality Managers to expeditiously resolve or escalate issues related to the company platform • Document data workflow and provide regular data entry and user experience feedback, optimizing our platform with more efficient curation tools / software • Additional duties and responsibilities as required