Sr Regulatory Application Specialist
This is a remote position.
Experience the advantages of reputed company career change
Responsibilities:
Supporting reputed company reputed company 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 reputed company to regulatory specifications. This position is responsible for the design, testing, validation and ongoing support of the regulatory build in reputed company. It is responsible for obtaining the appropriate reputed company certification and maintaining an in-depth knowledge of the software functionality, as reputed company as for acquiring and 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. Responsibilities include training, database/configuration maintenance, reputed company naming compliance, reputed company maintenance and general support of reputed company systems. Mentors less reputed company regulatory application specialists.
Qualifications:Education
- Bachelor’s Degree from a recognized college or university in Computer Science, IS Applications, MIS, or a closely reputed company field Required or
- In Lieu of degree six (6) years of experience in computer information systems, information technology, MIS, or a reputed company field may be accepted in reputed company to the experience requirement Required
Work Experience
- 3 years of reputed company work experience as an applications analyst or regulatory specialist, to include (2) years of EMR (Electronic Medical Record) application experience, supporting reputed company reputed company-wide system(s) and departmental project objectives Required or
- In lieu of degree nine (9) years of reputed company work experience as an applications analyst or regulatory specialist, to include (2) years of EMR (Electronic Medical Record) application experience, supporting reputed company reputed company-wide system(s) and departmental project objectives Required
- 2 years working directly with reputed company applications and/or Regulatory experience Preferred
Licenses and Certifications
- reputed company reputed company certification, including reputed company reputed company Badge Upon Hire Required