
11 - 50 employees
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
Biotechnology • Healthcare Insurance • Pharmaceuticals
N-Power Medicine, Inc. is a company focused on transforming the drug development process within the oncology field through an innovative clinical trial platform. Their solutions aim to accelerate oncology drug development by providing comprehensive, standardized data collection, expert staffing support, and real-time analysis capabilities. N-Power Medicine partners with oncologists, biopharma companies, and patient advocacy groups to overcome the challenges of slow drug development, limited clinical trial access, and suboptimal real-world data. By leveraging their N-Power Platform, they aim to unlock critical insights from routine care data, improve clinical trial adoption, and empower oncology practices to become high-performing research centers.
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11 - 50 employees
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
Biotechnology • Healthcare Insurance • Pharmaceuticals
N-Power Medicine, Inc. is a company focused on transforming the drug development process within the oncology field through an innovative clinical trial platform. Their solutions aim to accelerate oncology drug development by providing comprehensive, standardized data collection, expert staffing support, and real-time analysis capabilities. N-Power Medicine partners with oncologists, biopharma companies, and patient advocacy groups to overcome the challenges of slow drug development, limited clinical trial access, and suboptimal real-world data. By leveraging their N-Power Platform, they aim to unlock critical insights from routine care data, improve clinical trial adoption, and empower oncology practices to become high-performing research centers.
• Curate high-quality oncology datasets from various EHR platforms into proprietary or third-party EDC systems • Ensure compliance with NPM policies, SOPs, and GCP standards • Abstract comprehensive clinical information such as patient history, diagnosis, treatments, disease progression, and genomic results according to proprietary guidelines • Contribute to continuous process improvement by offering feedback on workflows, tools, and user experience • Collaborate with quality management and biostatistics to resolve data issues • Participate in the development of the platform by collaborating with data and software teams to innovate data collection • Availability during core business hours with flexibility to attend weekly team and company meetings as required • 90-100% of effort dedicated to abstraction depending on business need • Perform other duties as assigned to support team and company goals
• 3+ years of relevant experience with oncology data abstraction/curation from health information systems utilizing industry standard data ontologies • Bachelor’s degree preferred. Oncology Data Specialist (ODS) certification preferred • Oncology/Hematology RN/LPN, or Clinical Research Associate (CRA), or certified in an NCRA Accredited Program or comparable professional experience, preferred • Experience in both solid tumor and hematologic malignancy abstraction • Familiarity with genomic testing in cancer, preferred • Experience with OncoEMR and/or EPIC, preferred • Ability to navigate electronic health records (EHRs) and follow proprietary guidance documents to curate a comprehensive data set including, but not limited to, the history, diagnosis, treatment, and disease status for cancer patients • Self-starter with ability to prioritize in complex and fast-evolving environments and a drive to get things done • Technical savvy and a strong desire to learn new systems and technology • Attention to detail and strong organizational skills • Team player who enjoys a collaborative environment, with ability to problem solve and provide constructive and articulate feedback • Excellent oral/written communication & interpersonal skills • Strong desire to drive a paradigm change in clinical research conduct and improve the quality of care for cancer patients • Familiarity with HIPAA and FDA regulated clinical trials research requirements, preferred • Ability to work in a HIPAA-compliant home office • Generous, Curious, and Humble
• Company benefits for 30+ hours/week • Discretionary annual bonus based on performance • Equity at hire • Flexible work environment • 401K plan
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