Research Abstract Analyst III- Full time- Central Abstractor Office- One Ford Place

CHEManager International; Detroit (MI); On-site; USD 50,000 - 80,000; Full time

Job summary

CHEManager International in Detroit seeks a Data Abstraction Specialist to coordinate clinical data extraction from medical records for local, national and international research studies. You will monitor daily productivity, assure quality, and act as liaison between PI/Project Manager and the data collection team, using REDCap and Epic within established procedures.

The role requires an Associate or Bachelor degree in Health Information Management with professional credentials

Qualifications

• Associate degree in Health Information Management or related field with one of RHIT, RHIA, CTR, CCRP, RN.
• Bachelor's degree required; five years progressive experience.
• Knowledge of anatomy, physiology, pathophysiology, disease processes, medical terminology, pharmacology, and coding systems.
• Proficient in Microsoft Office (Excel, PowerPoint, Word, Access).
• Familiar with REDCap and Epic.
• Experience with web-based programs and databases (Midas, Quantros, CMS databases).
• Certifications/licensures: RHIT, RHIA, CTR, CCRP, RN.

Responsibilities

• Coordinate data collection team workflow for specified data collection initiatives.
• Monitor daily productivity in accordance with timeline.
• Provide quality assurance activities and coordinate auditing processes with PI.
• Function as liaison between PI/Project Manager and data collection team.
• Abstract clinical data from medical records for local, national and international research studies.
• Abstract data to satisfy compliance initiatives: COE's, P4P, Utilization Review, System Registries, Risk Adjustment, NHSN, HCC and Coding validation.
• Provide coding validation, consulting, and education.

Education

Bachelor's degree

Associate degree Health Information Management

RHIT

RHIA

CTR

CCRP

RN

Tools

Excel

PowerPoint

Word

Access

Job description

General Summary

• Coordinates data collection team workflow for specified data collection initiatives.
• Monitors daily productivity in accordance with timeline.
• Provides for quality assurance activities and coordinates auditing processes with PI.
• Functions as the liaison between PI/Project Manager and data collection team.
• Works autonomously using established procedures to interpret and abstract clinical data from the medical record for local, national and international research studies.
• Abstracts clinical data to satisfy numerous HFHS/HAP compliance and quality initiatives: COE's, P4P, Utilization Review, System Registries, Risk Adjustment, NHSN Infection control, Hospital Acquired Conditions, CMS Core Measures, CMS HCC and Coding validation.
• Provides coding validation, consulting, and education.

Education/Experience Required

• Associate degree Health Information Management or related field, in addition to maintaining one of the following credentials: RHIT, RHIA, CTR, CCRP, RN.
• Bachelor's degree required. Five (5) years progressive experience.
• Must have a thorough knowledge of anatomy, physiology, pathophysiology, disease processes, medical terminology, pharmacology, and coding systems.
• Working knowledge of Microsoft Office products - Excel, PowerPoint, Word, Access.
• Familiar with REDCap and Epic.
• Experience in accessing and utilizing web-based programs, for example, email, internet, vendor-based software as Midas, Quantros, CMS Pharmaceutical and Clinical Trial databases, etc.
• CERTIFICATIONS/LICENSURES REQUIRED: One of the following credentials: RHIT, RHIA, CTR, CCRP, RN.