
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.
6 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.
• 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.
• 3+ years of medical documentation and 6+ months in oncology/hematology experience • Bachelor’s degree or above in any healthcare related field strongly preferred • Experience in clinical research preferred; GCP certification is a plus • Extensive knowledge of the intricacies of provider documentation • Thorough understanding of medical terminology, facility workflow, efficiency management, and nuances of medical documentation • Strong computer skills with the ability to learn and navigate new software quickly • Excellent interpersonal skills including critical thinking and problem-solving • Strong prioritization, organizational and multitasking skills with attention to detail • Ability to function well in a fast-paced environment • Ability to work in a HIPAA-compliant home office • Strong written and verbal English communication • Ability to work in alignment with clinic hours • Ability to type 60 wpm preferred • Generous, Curious & Humble
• Equity at hire • Discretionary annual bonus • Company benefits at 30+ hours/week • Flexible work environment • 401K plan and other great company perks
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