N-Power Medicine, Inc.

Recruitment

• 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

Technical Recruiter

Director

• 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

Epidemiology Director

Clinical Research

• 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.

Senior Biostatistician

Operations

• Own the end-to-end delivery of executed life sciences contracts, ensuring all milestones, timelines, and deliverables are met or exceeded.
• Serve as the primary client contact for contract execution, managing relationships with pharma, biotech, and research partners throughout the project lifecycle.
• Lead cross-functional coordination efforts, bringing together teams from Clinical Operations, Epidemiology, Biostatistics, Product, Engineering, Data Science, and other internal stakeholders to deliver on contract commitments.
• Manage all project phases from kick-off through close-out, including regular client meetings, status updates, and comprehensive documentation of decisions and action items.
• Monitor project health through dashboards and management tools, proactively identifying and escalating risks, and driving resolution of critical project-related issues.
• Track and report key metrics to clients and internal stakeholders on a regular cadence, ensuring transparency and alignment throughout contract delivery.
• Champion process improvement initiatives, identifying opportunities to optimize workflows, reduce turnaround times, and enhance overall delivery efficiency.
• Advocate for the client experience across the organization, communicating feedback, product needs, and client sentiment to internal stakeholders.
• Foster strong relationships with key clients, ensuring their needs are met and proactively identifying opportunities to strengthen satisfaction and retention.
• Perform additional duties and responsibilities as required.

Staff Delivery Operations Manager

Solutions Engineer

• 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.

Solutions Architecture, GTM Strategy Director

Clinical Operations

• 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.

Clinical Research Operations Specialist

• Provide direct, day to day leadership for DHS assigned to a specific health system account
• Set clear expectations for performance, workflows, and professional behavior
• Monitor workload distribution and staffing coverage across assigned sites
• Address routine performance issues and escalate complex concerns to the Senior Manager
• Foster a positive, accountable, and high engagement team culture
• Partner with the Senior Manager to support hiring needs
• Own rapid and effective onboarding for new team members
• Identify onboarding gaps and recommend improvements to training processes
• Conduct regular check-ins and coaching conversations with direct reports
• Support ongoing skill development and role readiness
• Participate in performance reviews and contribute to promotion or corrective action discussions
• Monitor adherence to documentation, consent, and workflow standards
• Maintain strong working relationships with health system partners
• Perform additional duties and responsibilities as required.