Sr Regulatory Application Specialist

Responsibilities

• Supporting complex enterprise wide system(s) and departmental project objectives.
• Creating and controlling project plans, goals, deadlines, testing, implementation, changes, upgrades and post live support of assigned systems.
• Working with affected departments to ensure assigned systems reflect the regulatory environment and procedures are built to regulatory specifications.
• Designing, testing, validating and ongoing support of the regulatory build in Epic.
• Obtaining the appropriate Epic certification and maintaining an in-depth knowledge of the software functionality.
• Maintaining a working knowledge of the CMS provider regulatory programs (specifically MACRA for eligible clinicians and Promoting Interoperability for eligible hospitals) and its associated measure specifications.
• Training, database/configuration maintenance, standard naming compliance, security maintenance and general support of complex systems.
• Mentoring less experienced regulatory application specialists.

Qualifications

• Bachelor's Degree from a recognized college or university in Computer Science, IS Applications, MIS, or a closely related field.
• Required or In Lieu of degree: Six (6) years of experience in computer information systems, information technology, MIS, or a related field.
• Required Work Experience: Three (3) years of progressive work experience as an applications analyst or regulatory specialist, to include (2) years of EMR (Electronic Medical Record) application experience, supporting complex enterprise-wide system(s) and departmental project objectives.
• Required or In lieu of degree: Nine (9) years of progressive work experience as an applications analyst or regulatory specialist, to include (2) years of EMR (Electronic Medical Record) application experience, supporting complex enterprise-wide system(s) and departmental project objectives.
• Required: Two (2) years working directly with Epic applications and/or Regulatory experience.