DESCRIPTION/RESPONSIBILITIES:Job Description:HIS Clinical Analyst - Inpatient/Outpatient Methodology Groupers (New Health Care Company)This new Health Care Company will be a leading global diversified health technology company with:* Proven category leadership* Exposure to attractive end-markets* Innovation mindset driving improved patient outcomes* Collaborative customer relationships* Deep global regulatory experience* Operational excellence and strong cash flow* Strong sales growth and profitability with significant recurring sales
We expect the creation of the two companies will be completed by the end of the first quarter of 2024. We will continue to operate as one global company. This role is positioned to drive the success of the "New Health Care Company".
The Impact You'll Make in this RoleAs a HIS Clinical Analyst - Inpatient/Outpatient Methodology Groupers, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:* Assuming the primary responsibility of Clinical Analyst in providing subject matter expertise in the clinical content development, specification, documentation, validation, and application of software modules related to International Refined Diagnosis Related Groups (IR-DRGs), including Global growth of APR, EAPG and preventables, as well responsibility of maintaining the specifications of the map and any related mapping for IR-DRG and expansion of outpatient classification variables required for the methodology, holding to standards and best practices. This solution is used by throughout the world to budget, track, and pay for hospital inpatient and outpatient services.* Alignment of EAPG and IR-DRG outpatient, as well as the discipline of inpatient patient classification, procedure classification, inpatient payment, and regulatory update processes, demonstrating the underlying clinical concepts both in the US and international healthcare claim processing and payment policy* Work directly with the Chief Product Owner, Product Owners, Research team and government agencies to drive enhancements to the methodologies by reviewing proposed suggested changes, defining evaluation approach and specifications, review of results and proposal of recommendations towards updates to clinical logic that include clear clinical logic specifications using existing coding system definitions.* Work directly and collaborate with the technical, quality, and clinical team members, integrating product concepts to implement and test the clinical specification.* Responsible for maintaining process documentation for the IR-DRGs update using CandER standards and methods.
Work location: RemoteTravel: May include up to 5% domestic/internationalRelocation Assistance: Not authorized
Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).
Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.
3M is an equal opportunity employer. 3M will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.
Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.