Quality Manager

Decker Jones, P.C.; United States; Remote; USD 70,000 - 110,000; Full time

Job summary

A prominent healthcare institute is seeking a Quality Manager responsible for overseeing quality control aspects of oncology data abstraction projects. This role requires certification and experience in quality control, along with a commitment to maintaining high data standards. The position offers flexibility, remote work options, and a comprehensive benefits package including medical and retirement plans.

Benefits

Flexible schedule

Medical, dental, and vision benefits

Paid time off

Paid continuing education time off

401K retirement planning

Short-term disability

Company-paid life insurance and long-term disability

Qualifications

• At least two years of current ODS registry abstracting experience required.
• At least one year of current ODS quality control experience required.
• Intermediate skill level in computer software applications required.

Responsibilities

• Oversees quality control aspects of projects to ensure standards.
• Conducts re-abstraction and quality reviews weekly.
• Maintains project documentation and provides ongoing training.

Skills

Quality Control

Training

Data Management

Communication

Education

Associates’ or Bachelor’s degree in Health Information Management or related field

Tools

Cancer registry software systems

Job description

Quality Manager, ODS certified

This position oversees and directs the quality control (QC) aspects of assigned projects to ensure the Registry Partners (RP) standard of high-quality abstraction occurs. This includes working with other members of the management team to define the abstracting procedures, training and providing ongoing support to the ODS abstractors on assigned projects.

Essential Duties:

• Comply and follow the QC process as outlined and defined in the Quality Control Policy and Procedure.
• Conducts a re-abstraction of the initial cases for each ODS starting a new project.
• Conducts a weekly re-abstraction quality control review and/or quality control data report review for each ODS on assigned projects to ensure quality standards are consistently being met.
• Completes weekly case log verification for assigned projects, as outlined in Case log Verification Policy and Procedure.
• Monitors QC compliance and completion for assigned projects.
• Conducts all quality performance related coaching calls and participates in other quality performance related incident calls.
• Investigates and documents area of concerns/noncompliance issues as outlined in the Disciplinary Action Policy and Procedure.
• Works in collaboration with Registry Operations Manager or Accreditation Consultants on assigned projects.
• Creates and maintains project parameters and/or other project documentation to define the expectations and requirements for assigned projects.
• Prepares and provides training(s) to staff on assigned projects.
• Provides ongoing QC guidance and support to ODSs and analysts who are abstracting on assigned projects.
• Trains and monitors the performance of the Quality Analyst(s) assigned to the project.
• Communicate any client or staff concerns to the Sr. Registry Operations Services Director, Accreditation Services Director and Sr. Quality and Education Director.
• Submits abstracting/coding questions to the Cancer Forum or SEER Inquiry.
• Participates in internal and external educational activities, as requested.
  Ensures understanding and compliance with all updates/changes in the collection and coding of cancer data.
• Performs as a Project ODS, when needed.
• Provides timely response, per RP policy, to employee and client questions/concerns as needed.
• Attends and actively participates in conference calls, as requested.
• Fulfills committed work hours to meet the requirements of clients, employees and the company during normal business hours and a cross standard business days (Monday through Friday, 8:00 am to 5:00 pm in your time zone) and during non-standard hours (evenings, nights, weekends and holidays) as needed. Use of the company phone when out of office to maintain availability and assist with the expected response time, within four business hours of call, email or request for assistance. Completes timesheets and case logs in real time/daily and finalizes with signature by Sunday at midnight. Conducts timesheet completion reviews for assigned staff.

Compensation/Benefits:

All team members are employees of Registry Partners, not contractors. Employees have a flexible schedule, achieve a work/life balance, and can work remotely from all 50 states. Full-Time and Part-Time (30+ hours) staff members have peace of mind through our full-time guarantee and a full benefits package including:

• Competitive Pay
• Medical, dental, and vision benefits
  Paid time off
• Paid continuing education time off
• Paid holidays
• 401K retirement planning
• Short-term disability
• Company-paid life insurance and long-term disability

Registry Partners is a national provider of data abstraction, registry management, and consulting services. Proudly working remotely since we were founded in 2002.

We currently serve clients in over 40 states (employees in 43 states) and focus every day on our mission to improve the quality of our data collection processes, knowing that the data we process ultimately impacts the treatment and lives of patients within our communities and around the world.

• Oncology Data Specialist (ODS), required.
• At least two years of current ODS registry abstracting experience and use of all cancer registry industry related reference manuals, required.
• At least one year of current ODS quality control experience, required.
• At least two years of registry abstracting experience in a CoC program, preferred.
• At least two years of Registry Partner experience as Quality Analyst or Registry Operations Manager, preferred.
• National Accreditation Program for Breast Cancer (NAPBC) knowledge and experience, preferred.
• At least two years of registry management or other health related management experience, preferred.
• Associates’ or Bachelor’s degree in Health Information Management or related field, preferred.
• Intermediate skill level in computer software, industry related cancer registry software systems and EMR applications, required.