South Carolina’s largest and oldest health insurance company
RN Medical Affairs Coordinator
Location
United States
Posted
2 days ago
Salary
Not specified
No structured requirement data.
Job Description
Summary
Ensures that the Local Coverage Determination (LCD) process adheres to contract instructions. Creates, implements, and maintains educational tools to help providers reduce the submission of claims for non-covered services and reduce the claims payment error rate. The error rate is a factor in awarding and renewing Medicare/other contracts.
Description
Logistics
This position is full time (40 hours/week) Monday-Friday 8:00-5:00 and will be W@H.
Unrestricted RN license required
What You Will Do:
Provides clinical expertise, research, and judgment to develop Local Coverage Determinations(LCDS) under the direction of medical director. Maintains LCDS once developed.
Educates providers and internal customers on LCDS. Communicates with other interdepartmental staff in appropriate coding and reimbursement guidelines to ensure coordination and compliance.
Provides clinical input for internal requests. Serves as reviewer to determine inter-rater reliability.
To Qualify for This Position, You Will Need:
Bachelor's in a job related field OR Graduate of Accredited School of Licensed Practical Nursing or Licensed Vocational Nursing
Required Work Experience: 5 years clinical experience in medical insurance, managed care, case management, or claims management, or a combination of these areas.
Required Skills and Abilities: Knowledge of managed care or medical claims payment policy issues. Working knowledge of word processing, spreadsheet software. Excellent verbal and written communication skills. Excellent customer service, organizational, presentation, analytical or critical thinking skills. Ability to persuade, negotiate, or influence others. Ability to handle confidential or sensitive information with discretion.
Required Software and Tools: Microsoft Office.
Required License and Certificate: An active, unrestricted RN license from the United States and in the state of hire, OR, active compact multistate unrestricted RN license as defined by the Nurse Licensure Compact (NLC). For Division 33, Certified Genetic Counselor will be considered in lieu of RN License.
What We Prefer:
Bachelor's degree- Nursing.
7 years-clinical experience in medical insurance, managed care, case management, or claims management, or a combination of these areas.
Preferred Skills and Abilities: Working knowledge of database software. Knowledge of government/healthcare programs and contracts laws, regulations. Knowledge of government/healthcare programs and regulations, coding, and approval practices. Knowledge of corporate administrative/medical policy for all lines of business. Knowledge of guidelines, benefits, and coverage for all lines of business.
Preferred Software and Tools: Working knowledge of Microsoft Access or other database software, DB2 and Easytrieve.Preferred Licenses and Certificates: HIAA, Loma, and/or ACLI certification. MPH, MHA certifications.
Experience with molecular testing
Experience with policy work
What We Can Do for You:
401(k) retirement savings plan with company match.
Subsidized health plans and free vision coverage.
Life insurance.
Paid annual leave – the longer you work here, the more you earn.
Nine paid holidays.
On-site cafeterias and fitness centers in major locations.
Wellness programs and healthy lifestyle premium discount.
Tuition assistance.
Service recognition.
Incentive Plan.
Merit Plan.
Continuing education funds for additional certifications and certification renewal.
Equal Employment Opportunity Statement
BlueCross BlueShield of South Carolina and our subsidiary companies maintain a continuing policy of nondiscrimination in employment to promote employment opportunities for persons regardless of age, race, color, national origin, sex, religion, veteran status, disability, weight, sexual orientation, gender identity, genetic information or any other legally protected status. Additionally, as a federal contractor, the company maintains affirmative action programs to promote employment opportunities for individuals with disabilities and protected veterans. It is our policy to provide equal opportunities in all phases of the employment process and to comply with applicable federal, state and local laws and regulations.
We are committed to working with and providing reasonable accommodations to individuals with disabilities, pregnant individuals, individuals with pregnancy-related conditions, and individuals needing accommodations for sincerely held religious beliefs, provided that those accommodations do not impose an undue hardship on the Company.
If you need special assistance or an accommodation while seeking employment, please email mycareer.help@bcbssc.com or call 800-288-2227, ext. 47480 with the nature of your request. We will make a determination regarding your request for reasonable accommodation on a case-by-case basis.
We participate in E-Verify and comply with the Pay Transparency Nondiscrimination Provision. We are an Equal Opportunity Employer. Here's more information.
Some states have required notifications. Here's more information.
Related Guides
Related Categories
Related Job Pages
More Clinical Research Jobs
This role leads the design, development, and maintenance of clinical study databases for global medical device trials, serving as a technical expert for EDC platforms like Medidata. Responsibilities include leading database programming activities across the study lifecycle, developing custom reports, and acting as a systems administrator for clinical data platforms.
This role serves as the primary science lead for clinical trials, focusing on computerized cognitive testing and related services, while liaising with sponsors to address scientific data questions. Key duties include reviewing protocols, advising on software configuration, analyzing cognitive data, and authoring various scientific and monitoring reports.
The Senior CRA will monitor clinical trial sites to ensure strict adherence to study protocols, regulatory standards, and GCP guidelines, while conducting site visits to assess performance and resolve operational issues. Responsibilities also include collaborating with internal teams, providing guidance to site staff, and building strong relationships with site personnel to ensure successful trial execution.
The Senior CRA will monitor clinical trial sites to ensure strict adherence to study protocols, regulatory requirements, and GCP standards, while also conducting site visits to assess performance and resolve issues. They will collaborate with cross-functional teams, provide guidance to site staff, and build strong relationships with personnel to ensure smooth and successful trial execution.