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Clinical Data Abstractor III

Remote / Online - Candidates ideally in
Renton, King County, Washington, 98055, USA
Listing for: N-Power Medicine, Inc.
Remote/Work from Home position
Listed on 2026-07-02
Job specializations:
  • Science
    Clinical Research, Healthcare Compliance, Data Scientist
Salary/Wage Range or Industry Benchmark: 38572 - 46838 USD Yearly USD 38572.00 46838.00 YEAR
Job Description & How to Apply Below
Position: Clinical Data Abstractor III 2.11.26

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.

Position Overview

N‑Power Medicine is hiring a Clinical Data Abstractor III. In this position, you will curate high‑quality oncology datasets from various EHR platforms into proprietary or third‑party EDC systems while ensuring compliance with NPM policies, SOPs, and GCP standards. You will abstract comprehensive clinical information—such as patient history, diagnosis, treatments, disease progression, and genomic results—according to proprietary guidelines, contribute to continuous process improvement, and collaborate with quality management, biostatistics, data, and software teams to accelerate our platform and the collection of quality, regulatory‑grade clinical data.

This remote U.S. role offers a unique opportunity to grow professionally within a fast‑paced, mission‑driven startup.

Role Objectives and Responsibilities
  • Retrieve, abstract and curate high quality oncology data sets from various EHR platforms into a proprietary NPM or 3rd party electronic data capture (EDC) system.
  • Ensure compliance and confidentiality with NPM and Network Site policies, standard operating procedures (SOPs), and Good Clinical Practice (GCP).
  • Curate a comprehensive data set—including 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 regarding 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.
  • Maintain availability during core business hours with flexibility to attend weekly team and company meetings as required.
  • Dedicate 90‑100% of effort to abstraction depending on business need.
  • Perform other duties as assigned to support team and company goals.
Education, Experience, Behavioral Competencies, & Skills
  • 3+ years of relevant experience with oncology data abstraction/curation from health information systems utilizing industry standard data ontologies.
  • Bachelor’s degree preferred. Oncology Data Specialist (ODS) certification preferred.
  • Oncology/Hematology RN/LPN, Clinical Research Associate (CRA), or certification in an NCRA Accredited Program or comparable professional experience preferred.
  • Experience in both solid tumor and hematologic malignancy abstraction.
  • Familiarity with genomic testing in cancer preferred.
  • Experience with OncoEMR and/or EPIC preferred.
  • Ability to navigate electronic health records (EHRs) and follow proprietary guidance documents to curate a comprehensive data set.
  • 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.
  • Familiarity with HIPAA and FDA regulated clinical trials research requirements preferred.
  • Ability to work in a HIPAA‑compliant home office.
  • Generous, Curious, and Humble.
Travel Requirements

Ability to travel may be required from time to time.

Pay Information

The expected hourly range for this position is $28.00 to $34.00. Actual pay will be determined based on experience, qualifications, geographic…

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