Senior Medical Writer shaping key clinical and regulatory documents at Thermo Fisher Scientific. Collaborating with teams to drive strategy, quality, and execution of early - phase programs.
About the role
- Clinical Documentation Improvement Specialist educating clinicians on documentation and coding requirements. Collaborating across healthcare facilities and providing training to improve documentation quality.
Responsibilities
- Advise and educate Emergency Medicine, Hospital Medicine, Critical Care Medicine, Telemedicine, and Urgent Care internal and external clients on current documentation/coding requirements
- Counsel clinicians identified as outliers via face-to-face interaction, phone, web-based, and/or email
- Perform chart analysis/recommendations to support quality documentation feedback to clinicians
- Educate and counsel clinicians on how to resolve external chart queries
- Travel to territories as required to provide in-person documentation education and training
- Analyze coding and billing data to identify documentation and RVU outliers
Requirements
- Bachelor's degree - required in Health Information Management, Nursing, or another related field
- 2 years' experience in Hospital or Physician practice environment performing related job duties
- Experience with Emergency Medicine, Hospital Medicine, Urgent Care documentation and coding guidelines preferred
- Basic knowledge in Microsoft office suite
- Strong skills in Microsoft Suite such as Outlook, Excel, and PowerPoint
- Certification and Licenses: Registered Health Information Administration (RHIA), Documentation Improvement Practitioner (CDIP), Certified Clinical Documentation Specialist (CCDS), Certified Professional Coder (CPC), or Certified Coding Specialist (CCS)
Benefits
- Comprehensive benefits package
- Competitive compensation
- Health insurance
- 401(k) plan with company match
- Paid time off and holidays
- Professional development support
- Employee wellness resources
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