
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.
11 hours ago

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.
• 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
• 5+ years of relevant experience with data abstraction/curation (with Bachelors) or 3+ years of relevant data abstraction/curation (with Masters) • Bachelor’s degree in a related field • Certificate in Cancer Registry Management (CRM), Clinical Research Coordinator (CRC), Oncology Nursing (OCN) or Certified Tumor Registrar (CTR), preferred • Clinical oncology work experience in health information systems or clinical trials • Experience with data quality standards, clinical workflow, and FDA regulated, clinical trials research • Experience with clinical workflow in an oncology setting • Experience in biomarkers, cytogenetics, and hematopoietic cancers • Strong desire to drive a paradigm change in clinical research conduct and improve the quality of care for cancer patients • Self-starter with ability to prioritize in complex and fast-evolving environments and a drive to get things done • Attention to detail and strong organizational skills • Team player who enjoys mentoring and training new team members • Excellent oral/written communication and interpersonal skills • Generous, curious, and humble
• equity at hire • discretionary annual bonus based on Company performance • company benefits • competitive industry benefits • 401K plan
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