Clinical Data Abstractor III

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

Conduct pre-screening chart reviews via EHR/EMR systems and clinical sources to assess patient eligibility against protocol criteria

Maintain pre-screening logs and dashboards to document eligibility status

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, 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 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

90-100% of effort dedicated to abstraction depending on business need

Perform other duties as assigned to support team and company goals

Preferred

Bachelor's degree preferred

Oncology/Hematology RN/LPN, or Clinical Research Associate (CRA), or certified in an NCRA Accredited Program or comparable professional experience, preferred

Familiarity with genomic testing in cancer, preferred

Familiarity with HIPAA and FDA regulated clinical trials research requirements, preferred

Benefits

Equity at hire

A discretionary annual bonus which may be available based on Company performance

This position is eligible for company benefits at 30+ hours/week

A 401K plan

A balanced and flexible work environment

Competitive industry benefits

Other great company “perks.”

Cancer drug development platform using external control arms.

Redwood City, California, USA

https://www.npowermedicine.com

Growth Stage

Total Funding

$104M

Key Investors

Merck Global Health Innovation Fund

2026-09-01

Series B· $32M

2024-05-21

Series B· $72M

Leadership Team

Mark Lee

CEO & Co-Founder

Recent News

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2026-09-03

Venture Capital Firms

N-Power Medicine Closes $32 Million Series B Financing to Expand Its Community Oncology Network and Accelerate ProECA Adoption

Fortune

To get into Anthropic right now, you need at least $25 million. For OpenAI, it’s closer to $1 million.

Qualifications

3+ years of relevant experience with oncology data abstraction/curation from health information systems utilizing industry standard data ontologies

Experience in both solid tumor and hematologic malignancy abstraction

Familiarity with oncological clinical trial eligibility criteria and protocol review

Experience navigating EHR/EMR systems (e.g., Epic, Cerner, OncoEMR, Iknowmed) for chart review

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

Ability to work in a HIPAA-compliant home office

Applicants must be currently authorized to work in the U.S. on a full-time basis. The Company will not sponsor applicants for work visas

Bachelor's degree preferred

Oncology/Hematology RN/LPN, or Clinical Research Associate (CRA), or certified in an NCRA Accredited Program or comparable professional experience, preferred

Familiarity with genomic testing in cancer, preferred

Familiarity with HIPAA and FDA regulated clinical trials research requirements, preferred

Required skills

Oncology Data Abstraction, Solid Tumor and Hematologic Malignancy Abstraction, Clinical Data Curation, Health Information Data Ontologies, Clinical Trial Eligibility Criteria and Protocol Review, Epic, Cerner, OncoEMR, Iknowmed, Cancer Genomic Testing, HIPAA, FDA-Regulated Clinical Trials, Oncology/Hematology Nursing, Clinical Research Associate (CRA)

Preferred skills

Bachelor's degree preferred, Familiarity with genomic testing in cancer, preferred

Experience

3+ years