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

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.

Additional Information

• Organization: Corporate Services
• Department: Central Abstractor Office
• Shift: Day Job
• Union Code: Not Applicable