Clinical Data Abstractor/Curator III

Summary

Join N-Power Medicine as an Oncology Clinical Data Abstractor/Curator III and play a fundamental role in collecting and maintaining accurate cancer data for clinical trial candidate pre-screening. This remote position within the United States involves working with various EHR platforms, ensuring data quality and compliance, and collaborating with data and software teams. You will contribute to process improvement and data issue resolution. The ideal candidate possesses 3+ years of relevant oncology data abstraction experience and a Bachelor's degree is preferred. N-Power Medicine offers a competitive compensation package, including equity at hire, a discretionary annual bonus, and company benefits for those working 30+ hours per week.

Requirements

• 3+ years of relevant experience with oncology data abstraction/curation from health information systems utilizing industry standard data ontologies
• 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
• Ability to work in a HIPAA-compliant home office
• Excellent oral/written communication & interpersonal skills
• Generous, curious, and humble

Responsibilities

• Retrieve, curate and distribute quality data sets from various EHR platforms
• Ensure compliance and confidentiality with Company’s and site’s policies, standard operating procedures (SOPs), and Good Clinical Practice (GCP)
• 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 into process checks and interface with quality management and biostatistics to resolve data issues
• Availability during core business hours with flexibility to attend weekly team and company meetings as required
• Other duties as assigned

Preferred Qualifications

• Bachelor’s degree
• You are a Oncology/Hematology RN/LPN, or Clinical Research Associate (CRA), or certified in an NCRA Accredited Program or comparable professional experience
• Experience in both solid tumor and hematologic malignancy abstraction
• Experience with OncoEMR and/or EPIC
• Familiarity with genomic testing in cancer
• Familiarity with HIPAA and FDA regulated clinical trials research requirements

Benefits

• Equity at hire
• Discretionary annual bonus
• Company benefits at 30+ hours/week
• 401K plan