Role Description The Clinical Trials Office has an outstanding opportunity for a Clinical Research Billing Specialist to join their team. Reporting to the Clinical Research Billing Manager, the Clinical Research Billing Specialist supports the clinical research mission of UW Medicine by helping ensure accurate, compliant, and timely research billing and revenue cycle operations across a complex clinical trials portfolio. This role is a key resource within the Clinical Research Budget and Billing program, partnering with billing colleagues, study teams, practice sites, and other stakeholders to translate billing grids, Epic workflows, OnCore data, and Medicare rules into practical, high-quality operations. This is an opportunity to contribute to a central clinical research operation that helps bring important new therapies to patients while protecting UW Medicine from financial, regulatory, and reputational risk. The successful candidate will thrive in a fast-paced, collaborative environment; bring strong judgment and customer service; and enjoy solving complex billing and systems questions with accuracy, care, and a service-forward mindset. Key Responsibilities - Epic Research Billing Workflows (30%) - Review research billing activity to ensure charges route according to the study billing grid and Epic charge documentation, with attention to high-dollar and aging accounts. - Resolve charge review, claim edit, “No Rules,” and other escalated research billing questions in partnership with Research Billing Coordinators and other departments. - Epic Single Business Office (SBO) Research Invoicing Workflows (30%) - Support timely generation of SBO research invoices, including reviewing and processing invoice corrections and claims of missing charges. - Process invoice payments and follow up on aging research invoices to promote timely payment and accurate revenue cycle outcomes. - OnCore Clinical Trials Management System (CTMS)/Epic Interface (20%) - Ensure accurate handoff from OnCore to Epic when studies are activated, amended, or updated through subject enrollment changes. - Perform quality control of study and enrollment records and provide clear, constructive feedback to study teams as needed. - Patient Claims Review (10%) - Respond to questions about patients’ research study participation and the relationship between study activity and patient billing. - Identify trends or complex issues in patient claims review and escalate concerns to the Team Lead or Manager when appropriate. - Medicare Rules: Application and Training (10%) - Apply independent judgment in interpreting Medicare Clinical Trials Policy requirements and UW Medicine clinical research budgeting and billing policies and procedures. - Provide accurate guidance, training, and customer service to CRBB colleagues, investigators, research staff, and practice site partners on research billing policies, procedures, and tools. Qualifications - Bachelor’s degree in science, business, healthcare administration, or a related field and at least two years of related experience, or an equivalent combination of education and experience. - Applicants who do not meet these qualifications WILL NOT be forwarded to the Hiring Manager. Requirements - Prior experience with Epic Resolute, including hospital and/or professional billing workflows. - Demonstrated team leadership skills and the ability to make positive contributions in a collaborative, high-volume work environment. - Exceptional customer service, written communication, oral presentation, and stakeholder engagement skills. - Ability to understand, interpret, and communicate complex policy, financial, scientific, and technical information to a broad audience. - Ability to teach, mentor, prioritize, and organize work independently in a fast-paced environment. - Demonstrated skill using Microsoft Excel and Access. Preferred Qualifications - Five years of experience in healthcare and/or research billing, clinical research study coordination or management, health system operations, or related research or healthcare experience. - Experience in an academic medical setting. - Experience with Epic Research Billing and/or a clinical trials management system, preferably OnCore. - Accounting or finance experience. - Knowledge of Medicare Clinical Trials Policy and other federal, state, and institutional clinical research regulations. Benefits - Pay Range Minimum: $66,000.00 annual - Pay Range Maximum: $84,000.00 annual - For information about benefits for this position, visit https://www.washington.edu/jobs/benefits-for-uw-staff/ - Shift: First Shift (United States of America) - Temporary or Regular? This is a regular position - FTE (Full-Time Equivalent): 100.00% - Union/Bargaining Unit: Not Applicable

Role Description Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. This is a role well suited to an ambitious professional, looking for the next step in their career. As a Clinical Innovation & Informatics, Imaging Expert: - You will analyze customers’ business requirements within complex healthcare environments by applying data and workflow process knowledge to technology roadmap/enabling objectives. - You will manage customer engagements to drive measurable, sustainable improvements in clinical, operational, and financial outcomes. - You will lead and support project teams and conduct status checks with the customer to assess progress against plans and timelines to successfully meet the goals of the engagement. - You will prepare and present project status reports and assist in sales support interactions. This position may suit you best if you are familiar with the following: - You have working knowledge of current trends in healthcare, including value-based healthcare, and population health management. - You have knowledge of radiology economics, budgeting process, and financial planning. - You have engagement management, project/program management and/or consulting experience in a performance improvement environment. - You demonstrate an applied understanding of analytics and workflow optimization. - You have professional oral and written presentation skills in the customer environment, and you demonstrate team and customer orientation. - You have good PC skills (MS Office software like Word, PowerPoint, Excel, and Outlook). - You will be working with our latest technology and therefore you are willing to learn about new software and hardware solutions. - You have a deep understanding of imaging clinical workflows and associated processes. - You have experience with imaging informatics as it relates to the imaging value stream. - You have strong understanding of quality improvement initiatives including quality control activities. Qualifications - Imaging credentials with a Bachelor’s Degree in Clinical Healthcare related field. - Advanced Degree in a related business, management, communications, or clinical healthcare field preferred. - Minimum 8-10 years of combined clinical and management experience in a healthcare setting. - Willing to travel up to 60%. Benefits - Medical insurance - Dental insurance - Vision insurance - 401(k) retirement plan - Life insurance - Long-term and short-term disability insurance - Paid parking/public transportation - Paid time off - Paid sick and safe time

Role Description Kentro is hiring an experienced Sr. Clinical Informaticist to support the Department of Veterans Affairs. As a Clinical Informaticist supporting the Clinical Process Modeling (CPM) and VistA Sustainment program within the Veterans Health Administration, you will be responsible for: - Supporting the day-to-day execution of the CPM project. - Providing professional and technical Health Informatics (HI) services to support the development of enterprise CPM Blueprints and related Clinical Decision Support workflows. - Working with clinical analysts, program analysts, health systems specialists, and information architects to provide health informatics expertise and develop CPMs for implementation in legacy VistA and Cerner environments. - Supporting the transition to the Cerner electronic health record (EHR) at VA Medical Centers (VAMCs). - Involvement in organizational change management, support of Initial Operating Capability (IOC), and CPM Blueprints efforts. Responsibilities - Work with a cross-functional team of SMEs, CACs, and clinical professionals to assess, analyze, and design clinical workflows related to CPRS/VistA & Cerner transition. - Provide domain-specific expertise focused on research, data gathering, and data analysis for the development of CPM Blueprints. - Collaborate with Government staff and other potential SME teams to determine clinical needs for Clinical Decision Support (CDS) workflow processes. - Provide inputs to documents for EHR training with appropriate terminology, graphics, and examples. - Assist with ensuring clinical terminology in future CPM Blueprints is accurate. - Research and identify content for, document design and logic of, and create and validate government-designated CPM processes. - Coordinate tasks/activities within specific clinical program offices. - Conduct publication/NCBI research. - Consolidate clinical and evidence-based best practices. - Work with terminologists and clinical informaticists on analyzing clinical concepts and data standards. - Consult medical literature, clinical texts, guidelines, SMEs, and other authoritative sources in the development of CPM blueprints. - Conduct research and gather data on ancillary packages in coordination with clinical analysts. Qualifications - Degree in Medicine, nursing, bioinformatics, or health science. - Direct experience working with Veterans Health Affairs' customers/healthcare providers. - Minimum of ten years' experience working as a clinical informaticist on healthcare-related projects. - Knowledge of direct patient care environments and clinical topics covered by the CPM Blueprints. - Understanding of the clinical setting, clinical practice, clinical informatics, and prevailing standards. - Skilled in MS Forms, MS PowerPoint, MS Excel, SharePoint, reporting and analytics tools. Preferred Qualifications - Excellent verbal and written communication skills. - Experience supporting health IT-related projects. - Experience leading clinical informatics research, data gathering, and analysis tasks. - Experience validating, interpreting, and analyzing clinical concepts, data, and trends. - Experience interfacing directly with clients. - Direct experience with electronic health record technologies and implementations (specifically Cerner). - Direct experience with clinical process modeling. Clearance Requirement - US Citizen or Green card holder. - Willing and able to obtain and maintain Public Trust Clearance. - Must meet updated ID requirements. Benefits - Competitive benefits package including paid time off, healthcare benefits, and supplemental benefits. - 401k including an employer match. - Education reimbursement for certifications, degrees, or professional development. - Flexibility for professional growth and networking. - Funds for activities – virtual and in-person, including happy hours and holiday events. - Commitment to a positive workspace fostering creativity and innovation. Commitment to Equal Opportunity Employment Kentro is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to disability, status as a protected veteran, or any other status protected by applicable federal, state, or local law. How to Apply To apply to Kentro Positions, please click on the job link and then click the blue “Apply” button at the top right of Job Description. Please upload your resume and complete all the application steps. Accommodations Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform essential functions. If you need to discuss reasonable accommodations, please email careers@kentro.us.

• Leads the statistical design, analysis, interpretation, and reporting of pharmacovigilance and safety-focused observational studies using complex longitudinal registry data • Collaborates with investigators, epidemiologists, clinicians, and clients to develop protocols, Statistical Analysis Plans (SAPs), and analytic strategies that support client objectives and regulatory commitments • Independently performs advanced statistical analyses and sample size/power calculations in accordance with SAPs and industry best practices • Provides strategic statistical leadership and independently makes sound statistical decisions related to safety analyses and real-world evidence generation • Oversees and mentors Biostatistician I/II analysts and other junior staff, ensuring quality, accuracy, and consistency of statistical analyses and documentation • Develops and implements standardized methodologies, analytical templates, and programming approaches to improve efficiency, reproducibility, and consistency across projects