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11 days
Not Specified
Not Specified
$24.78/hr - $38.85/hr (Estimated)
<p>At Moffitt Cancer Center, we strive to be the leader in understanding the complexity of cancer and applying these insights to contribute to the prevention and cure of cancer. Our diverse team of over 9,000 are dedicated to serving our patients and creating a workspace where every individual is recognized and appreciated. For this reason, Moffitt has been recognized on the 2023 Forbes list of America's Best Large Employers and America's Best Employers for Women, Computerworld magazine's list of 100 Best Places to Work in Information Technology, DiversityInc Top Hospitals & Health Systems and continually named one of the Tampa Bay Time's Top Workplace. Additionally, Moffitt is proud to have earned the prestigious Magnet designation in recognition of its nursing excellence. Moffitt is a National Cancer Institute-designated Comprehensive Cancer Center based in Florida, and the leading cancer hospital in both Florida and the Southeast. We are a top 10 nationally ranked cancer center by Newsweek and have been nationally ranked by U.S. News & World Report since 1999.</p> <p>Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. Join our committed team and help shape the future we envision.</p> <p>Summary</p> <p>Position Highlights:</p> <p>The Research Financial Compliance Auditor II is responsible for the clinical research revenue lifecycle, including budget and coverage analysis for clinical trials, and research billing activities for Moffitt Cancer Center. Under the direction of the Research Financial Compliance Officer, the Research Financial Compliance Auditor II will prepare, schedule, and conduct audits of investigator initiated, pharma, and medical device clinical trials, and perform detailed research billing audits and other identified areas, including reports and follow-up, to ensure compliance with applicable regulations, GCP guidelines, and organizational quality standards.</p> <p>The Research Financial Compliance Auditor II is responsible for conducting special complex reviews for allegations of research or clinical trials billing non-compliance and assist with targeted training to team members, investigators, and administrators to ensure compliance with federal, state, and local laws and hospital policies relating to billing of research trials. This position will also provide general support to the Research Financial Compliance program as needed.</p> <p>Responsibilities:</p> <ul> <li>Prepares, schedules, and conducts coverage analysis and clinical research billing audits; analyzes allocation of charges and billing processes to ensure compliance with applicable regulations, and organizational quality standards. </li><li>Recommends corrective action(s) to improve deficiencies and communicates recommendations to the appropriate team members, department administrators, management, and others as needed. </li><li>Contributes clinical research revenue lifecycle policies, information, tools, and resources on the website and other forums. </li><li>Provides support to the Research Financial Compliance program as needed. </li><li>Stays abreast of federal, state, and local developments and compliance efforts related to research billing and clinical trials. </li><li>Maintains appropriate certifications. Remains up to date on changes to regulations relating to clinical trial billing and effectively communicate both verbally and in writing. </li><li>Strong analytical and problem-solving skills with attention to detail. </li><li>Ability to work with all levels, and within a strong team environment. </li><li>Proficient in using computer software applications such as Microsoft Excel, Word, PowerPoint, and Adobe. </li><li>Investigates reports related to research billing and other related research noncompliance. </li><li>Prepares, schedules, and conducts audits of clinical research finance activities for compliance in accordance with all applicable regulations and organizational quality standards. </li><li>Track audits and CAPAs in Corporate Compliance Software program. </li></ul> <p>Credential and Qualifications:</p> <ul> <li>Bachelor's Degree in Business Administration, Health Information Management, Health Sciences, Healthcare Administration, Research Administration, Accounting/Finance required. </li></ul> <p>In lieu of a Bachelor's Degree, an Associate Degree with 3 years of additional clinical research billing compliance or research finance/operations experience is required.</p> <ul> <li>1 year auditing experience required. </li><li>3 years of clinical research billing compliance or research finance/operations experience required. </li><li>Thorough understanding of coding requirements and current applicable laws and regulations, including federal, state, and non-federal regulations surrounding research and Medicare and/or third-party payor reimbursement. </li><li>Detailed knowledge of clinical services billing and processing, including the understanding of hospital billing and physician billing. </li><li>Thorough knowledge of ICH Guidelines, GCPs, and FDA Code of Federal Regulations and other applicable regulatory authority laws and regulations as they pertain to the conduct of clinical trials, e.g., pharma, medical device, clinical trials billing requirements. </li><li>Experience with EHR, CTMS or other tracking mechanisms, and Physician & Hospital Billing Systems. </li><li>Knowledge and understanding of the grants management lifecycle for research. </li></ul> <p>Preferred Experience:</p> <ul> <li>4 years of clinical research billing compliance experience including coding, billing, or revenue cycle functions or clinical research finance experience in an academic medical center, health system, or research institute preferred. </li><li>2 years of quality monitoring or auditing activities in an academic medical center, health system, or research institute preferred. </li><li>Familiarity with Good Clinical Practice (GCP) guidelines. </li><li>Coding or revenue cycle experience. </li><li>Professional certification applicable to compliance or clinical research (i.e. CHRC, CHC, CGMS, SOCRA, ACRP, NCURA, NRA). </li><li>Advanced skills with spreadsheets and data analytics. </li></ul> <p>Share:</p>
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