Clinical Data Abstractor III

3 hours, 17 minutes ago
Full-time
Mid Level
Data Science and Analytics
N-Power Medicine

N-Power Medicine

N-Power Medicine accelerates drug development by creating a research-ready network that integrates standard of care patients and diverse populations into clinical trials, facilitating informed decision-making for phase II to phase III studies in oncology.

Biotechnology
11-50
Founded 2021

Description

  • Retrieve, abstract, and curate oncology datasets from EHR platforms into NPM or third-party EDC systems.
  • Conduct pre-screening chart reviews to assess patient eligibility against clinical trial protocols.
  • Maintain prescreening logs and eligibility dashboards.
  • Abstract patient history, diagnoses, treatments, disease progression, and genomic results using proprietary guidelines.
  • Ensure compliance with NPM policies, SOPs, confidentiality requirements, and GCP standards.
  • Provide feedback on abstraction workflows, tools, educational resources, features, and user experience.
  • Collaborate with quality management and biostatistics teams to resolve data issues and improve process checks.
  • Partner with data, software, quantitative science, and data development teams to improve platform functionality and data collection.
  • Dedicate approximately 90–100% of effort to abstraction based on business needs and support additional team priorities.

Requirements

  • 3+ years of experience abstracting or curating oncology data from health information systems using industry-standard data ontologies.
  • Experience abstracting both solid tumor and hematologic malignancies.
  • Familiarity with oncology clinical trial eligibility criteria and protocol review.
  • Experience navigating EHR/EMR systems such as Epic, Cerner, OncoEMR, or Iknowmed.
  • Ability to curate comprehensive cancer data by following proprietary guidance documents.
  • Bachelor’s degree preferred.
  • Oncology/hematology RN or LPN, Clinical Research Associate, NCRA-accredited certification, or comparable professional experience preferred.
  • Familiarity with cancer genomic testing, HIPAA, and FDA-regulated clinical trial requirements preferred.
  • Strong attention to detail, organization, communication, problem-solving, and collaboration skills.
  • Ability to work independently in a fast-changing environment, attend core-hours meetings, maintain a HIPAA-compliant home office, and travel less than 10%; U.S. work authorization required without visa sponsorship.

Benefits

  • Remote position within the United States with a flexible work environment.
  • Hourly pay range of $28.00–$34.00, based on experience, qualifications, and location.
  • Equity offered at hire.
  • Potential discretionary annual bonus based on company performance.
  • Company benefits available for employees working 30 or more hours per week.
  • 401(k) plan and competitive industry benefits.

Interested in this position?

Apply directly on the company website

Apply Now

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