Medical Biller for Healthcare Organization focusing on Sickle Cell Disease

Job Posted: 12.09.2021 22:29:59

We are seeking a Medical Biller that can ensure that our claims are ready for billing, and that patients are up to date in their payments.

Job Responsibilities:

-Ensures that encounters in EHR have all necessary codes and attachments and mark them as ready for the billing company. Coding experience is required for this position.
-Generates revenue by making payment arrangements, collecting accounts, and monitoring and pursuing delinquent accounts.
-Collects delinquent accounts by establishing payment arrangements with patients, monitoring payments, and following up with patients when payment lapses occur.
-Maintains Medicare bad-debt cost report by tracking billings, monitoring collections, and compiling information.
-Maintains work operations by following policies and procedures, and reporting compliance issues.
-Maintains quality results by following standards.
-Protects FSCDR’s value by keeping collection information confidential.
-Updates job knowledge by participating in educational opportunities.
-Serves and protects the clinical community by adhering to professional standards, hospital or clinic policies and procedures, federal, state, and local requirements and standards.
-Enhances billing department and practice reputation by accepting ownership for accomplishing new and different requests and exploring opportunities to add value to job accomplishments.

About the Foundation for Sickle Cell Disease Research

We are fighting a battle for people living with Sickle Cell Disease (SCD). The Foundation for Sickle Cell Disease Research (FSCDR) is the United States’ first outpatient center exclusively dedicated to the treatment of and innovative research for SCD. Florida has the highest population of individuals living with SCD in the U.S. In 2012, we opened our first center in Hollywood, FL, offering focused care and collecting data through clinical trials. We utilize a human-centric, community-based, rigorously scientific approach to caring for our patients and finding better solutions to treat them.

For the past seven years, we have grown strong roots in the South Florida community and have taken great strides toward our mission of resetting the narrative around SCD through specialized care and innovative research.

We are focused on helping people living with SCD—offering more support to our patients, their families, and the broader sickle cell trait and advocate communities, while creating a center for collaborative research that encourages scientists, medical professionals, and physicians researching and treating SCD to work toward new, life-improving solutions.

We are a woman-owned and black-owned organization and we are expanding! We have big
plans in store!

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