Clinical Data Abstractor III 2.11.26

3 weeks, 4 days 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 high-quality oncology datasets from various EHR platforms into proprietary or third-party EDC systems.
  • Ensure compliance with N-Power Medicine policies, SOPs, GCP standards, and confidentiality requirements.
  • Abstract comprehensive oncology data, including patient history, diagnosis, treatment regimens, disease progression, and genomic testing results.
  • Follow proprietary abstraction guidelines to produce complete and accurate clinical datasets.
  • Provide feedback and recommendations to improve abstraction workflows, user experience, educational resources, features, and tools.
  • Partner with quality management and biostatistics to identify, review, and resolve data issues.
  • Collaborate with Clinical Science to define key data elements and abstract unstructured data from multiple EHR sources.
  • Work with Software Engineering to improve the data collection experience and optimize UI/UX.
  • Maintain availability during core business hours and participate in weekly team and company meetings as needed.
  • Perform other duties as assigned in support of team and company goals.

Requirements

  • 3+ years of relevant experience with oncology data abstraction or curation from health information systems using 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 preferred, or comparable professional experience.
  • Experience with both solid tumor and hematologic malignancy abstraction.
  • Familiarity with genomic testing in cancer preferred.
  • Experience with OncoEMR and/or EPIC preferred.
  • Ability to navigate EHRs and follow proprietary guidance documents to curate complete cancer patient data.
  • Strong organizational skills, attention to detail, and ability to prioritize in fast-changing environments.
  • Excellent oral and written communication and interpersonal skills.
  • Ability to work in a HIPAA-compliant home office.
  • Familiarity with HIPAA and FDA-regulated clinical trials research requirements preferred.
  • Must be authorized to work in the U.S. on a full-time basis; no work visa sponsorship is available.
  • Availability during core business hours with flexibility for weekly team and company meetings.
  • Ability to travel occasionally as needed.

Benefits

  • Hourly pay range of $28.00 to $34.00, based on experience, qualifications, and location.
  • Equity at hire.
  • Discretionary annual bonus based on company performance.
  • Company benefits eligibility at 30+ hours per week.
  • 401(k) plan.
  • Balanced and flexible work environment.
  • Competitive industry benefits.
  • Remote position within the United States.

Interested in this position?

Apply directly on the company website

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