Clinical Data Abstractor/Curator IV 2.4.26

About N-Power Medicine   N-Power Medicine aims to establish a new paradigm in drug development by reinventing the ‘how’ and transforming clinical trials through better integration with clinical practice, ensuring broader participation by physicians and patients.  We are building an exceptional multi-disciplinary team with diverse expertise spanning healthcare, engineering, technology and regulatory, and with people who share our core value of Empowering Community through generosity, curiosity and humility.  We are working with urgency to bring better therapies to patients faster. About N-Power Medicine N-Power Medicine aims to establish a new paradigm in drug development by reinventing the ‘how’ and transforming clinical trials through better integration with clinical practice, ensuring broader participation by physicians and patients.  We are building an exceptional multi-disciplinary team with diverse expertise spanning healthcare, engineering, technology and regulatory, and with people who share our core value of Empowering Community through generosity, curiosity and humility.  We are working with urgency to bring better therapies to patients faster.  Position Overview N-Power Medicine is hiring an Oncology Clinical Data Abstractor/Curator IV This position will have a fundamental role in collecting and maintaining comprehensive and accurate cancer data used to pre-screen candidates for clinical trials. You will be a part of a dynamic data abstraction team with the opportunity to impact the future of clinical research and improve patients’ lives, while growing professionally at a dynamic, fast-growing, start-up organization. You will contribute to the development of our platform by collaborating with our data and software teams to accelerate and innovate our platform and the collection of quality, regulatory-grade clinical data. This position is remote within the United States. Role Objectives and Responsibilities -Retrieve, abstract and curate high quality oncology data sets from various EHR platforms into an electronic data capture (EDC) system -Ensure compliance and confidentiality with Company’s and network site’s policies, standard operating procedures (SOPs), and Good Clinical Practice (GCP) -Curate a comprehensive data set including, but not limited to, patient history, diagnosis, treatment regimens, disease progression and genomic testing results according to proprietary abstraction guidelines -Participate in the continual improvement of processes by providing feedback and recommendations pertaining to abstraction workflows, user experience, educational resources, features, and tools -Provide input on workflow improvements, user tools, documentation and abstraction best practices -Mentor and support new and existing team members, providing guidance on abstraction workflows and clinical content -Involvement with data quality assurance activities  -May assist with monitoring and prioritizing case assignments and team productivity -Support technology advancement efforts to improve data flow and abstraction efficiency -Availability during core business hours with flexibility to attend weekly team and company meetings as required -Perform other duties as assigned to support team and company goals   Education, Experience, Behavioral Competencies, & Skills -5+ years of relevant experience with oncology data abstraction/curation from health information systems utilizing industry standard data ontologies -Bachelor’s degree preferred -Oncology/Hematology RN, LPN, Clinical Research Associate (CRA), Oncology Data Specialist (ODS) credential or equivalent professional experience, preferred -Experience in both solid tumor and hematologic malignancy abstraction  -Experience abstracting cancer genomic testing data, required -Experience with OncoEMR and/or EPIC, preferred  -Self-motivated with the ability to prioritize tasks in a dynamic and fast-evolving environment -Technical savvy and a strong desire to learn new systems and technology -Attention to detail and strong organizational skills -Solutions-oriented team player who offers developmental feedback and drives quality  -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 effectively in a HIPAA-compliant home office -Excellent oral/written communication & interpersonal skills -Generous, curious, and humble Travel Requirements  - Up to 5% of time required to travel in role (out of 100%)