Clinical Data Abstractor/Curator IV

Summary

Join N-Power Medicine as an Oncology Clinical Data Abstractor/Curator IV! This remote position within the United States plays a crucial role in collecting and maintaining accurate cancer data for clinical trial candidate pre-screening. You'll be part of a dynamic team, impacting clinical research and patient lives while growing professionally in a fast-paced startup. Responsibilities include data retrieval, curation, and distribution from various EHR platforms, ensuring compliance and confidentiality. You will also contribute to process improvement and mentor team members. This role requires 5+ years of relevant oncology data abstraction experience and expertise in cancer genomic testing data. A Bachelor's degree is preferred, along with experience with OncoEMR and/or EPIC. N-Power Medicine offers competitive compensation, including equity at hire and a discretionary annual bonus, along with benefits for those working 30+ hours per week.

Requirements

• 5+ years of relevant experience with oncology data abstraction/curation from health information systems utilizing industry standard data ontologies
• Experience abstracting cancer genomic testing data, required
• 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
• Mentoring and training of new and existing team members
• Involvement with data quality assurance activities
• May assist with monitoring and prioritizing case assignments and team productivity
• Champion technology advancements for internal workflow improvement
• 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, preferred
• You are a Oncology/Hematology RN/LPN, or Clinical Research Associate (CRA), or certified in an NCRA Accredited Program or comparable professional experience, preferred
• Experience in both solid tumor and hematologic malignancy abstraction
• Experience with OncoEMR and/or EPIC, preferred
• Familiarity with HIPAA and FDA regulated clinical trials research requirements, preferred

Benefits

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