8 дней назад
Senior Clinical Data Abstractor (Oncology)
35 - 40$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Clinical Data Abstractor (Oncology): Abstracting and standardizing complex clinical patient data from electronic health records, paper charts, and other source documents for research, quality improvement, and regulatory reporting with an accent on medical coding, data management, and clinical data quality. Focus on interpreting unstructured medical records, supporting AI and LLM prompt engineering, maintaining compliant ETL workflows, and conducting peer reviews for accurate encoded data.
Location: US Remote; U.S. licensure required
Salary: $35–$40 per hour
Company
develops cell-free DNA testing and genetic diagnostics for oncology, women’s health, and organ health.
What you will do
- Review, interpret, and abstract clinical patient data from EHR systems, paper charts, and other source documents.
- Apply medical coding systems and clinical standards to classify unstructured information into standardized, machine-readable data.
- Enter, track, and maintain clinical data in REDCap, registries, and custom electronic data capture systems.
- Support clinical data management, ETL workflows, quality assurance, and regulatory reporting.
- Support AI and LLM initiatives, including prompt engineering and translating clinical data requirements for cross-functional teams.
- Conduct peer reviews, contribute to process improvements, and deliver regular abstraction and productivity reports.
Requirements
- U.S.-licensed Nurse, PA-C, NP, or DNP with a Master’s degree in health sciences required.
- Four to five years of experience in clinical data abstraction and medical records review, preferably in cancer, women’s health, or rare diseases.
- Experience with clinical data encoding, ICD-10-CM, SNOMED CT, data mapping, standardization, and harmonization.
- Knowledge of medical terminology, disease processes, clinical workflows, genetic testing, HIPAA, and clinical data privacy requirements.
- Proficiency with Microsoft Office or Google Workspace, pivot tables, reporting, data analysis, and clinical data systems.
- Ability to work independently, manage priorities, collaborate across clinical and non-clinical teams, and meet productivity and quality deadlines.
Nice to have
- Experience in oncology, women’s health, or rare diseases.
- CCDM, CCRP, ACR-P, or CRA certification.
Culture & Benefits
- Medical, dental, vision, life, and disability benefits for eligible employees and dependents.
- Free testing for employees and immediate family members, plus fertility care benefits.
- Pregnancy and baby bonding leave, 401(k), commuter benefits, and an employee referral program.
- Work with statisticians, geneticists, physicians, laboratory scientists, software engineers, and other clinical and technical professionals.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →
Похожие вакансии
10 дней назад
Medical Coder (Clinical Trials)
80 000 - 105 000$
9 дней назад
Senior Cancer Registrar (Part-Time Consultant / Domain Advisor)
20 - 40$
14 дней назад
Regulatory Affairs Coordinator (Clinical Research)
65 000 - 95 000$
9 дней назад
Senior Clinical Trials Manager (Biotech)
143 000 - 157 300$
9 дней назад
Associate Medical Director or Medical Director (Oncology)
216 000 - 270 000$
10 дней назад
Senior GCP Auditor (Biotech)
140 000 - 154 000$