Job Details Description The is a professional association serving nearly 40,000 members across the country. Consistent with the ACR’s mission to advance the practice of radiology and improve the health outcomes of the populations we serve, the ACR’s Center for Research and Innovation (C...
Description: ***Working on a remote basis is applicable to only those in Eastern and Central US Time Zones*** Description\: As an Auditor in our Corporate Department Quality Medicine (QM), you will perform Good Clinical Practice (GCP) audits mainly in the areas of biostatistics, clinical data...
Piper Clinical Solutions is seeking motivated professionals for a Remote Healthcare Claims Quality Assurance Auditor opportunity with a national Health Insurance Organization. The Healthcare Claims Quality Assurance Auditor will support ongoing claims audit operations to ensure strong quality f...
Responsibilities REMOTE- Professional Coding Auditor The Professional Coding Auditor provides quality documentation review and analysis to support accuracy of coding documentation. Reviews professional encounters to compare CPT E/M levels and ICD-10 diagnosis codes to the physicians’ docum...
Overview The Coding Quality Auditor will be responsible for performing Diagnostic Related Group (DRG) validation and ensuring the coding quality of charts reviewed by the Physician Teams, a two-person team consisting of an MD Reviewer and a Coding Quality Expert (CQE). Coding Quality Auditor will do...
The Clinical Review Auditor is responsible for performing accurate Clinical Validation Audits of inpatient medical records to validate diagnoses. The Clinical Review Auditor also screens claim data and responds to provider appeals. The Clinical Review Auditor works closely with DRG Analysts and p...
The Clinical Review Auditor is responsible for performing accurate Clinical Validation Audits of inpatient medical records to validate diagnoses. The Clinical Review Auditor also screens claim data and responds to provider appeals. The Clinical Review Auditor works closely with DRG Analysts and p...
The Clinical Review Auditor is responsible for performing accurate Clinical Validation Audits of inpatient medical records to validate diagnoses. The Clinical Review Auditor also screens claim data and responds to provider appeals. The Clinical Review Auditor works closely with DRG Analysts and p...
The Clinical Review Auditor is responsible for performing accurate Clinical Validation Audits of inpatient medical records to validate diagnoses. The Clinical Review Auditor also screens claim data and responds to provider appeals. The Clinical Review Auditor works closely with DRG Analysts and p...
The Clinical Review Auditor is responsible for performing accurate Clinical Validation Audits of inpatient medical records to validate diagnoses. The Clinical Review Auditor also screens claim data and responds to provider appeals. The Clinical Review Auditor works closely with DRG Analysts and p...
The Clinical Review Auditor is responsible for performing accurate Clinical Validation Audits of inpatient medical records to validate diagnoses. The Clinical Review Auditor also screens claim data and responds to provider appeals. The Clinical Review Auditor works closely with DRG Analysts and p...
Responsibilities REMOTE- Professional Coding AuditorThe Professional Coding Auditor provides quality documentation review and analysis to support accuracy of coding documentation. Reviews professional encounters to compare CPT E/M levels and ICD-10 diagnosis codes to the physicians' documentation to...
Responsibilities:REMOTE- Professional Coding AuditorThe Professional Coding Auditor provides quality documentation review and analysis to support accuracy of coding documentation. Reviews professional encounters to compare CPT E/M levels and ICD-10 diagnosis codes to the physicians documentation to ...
SUMMARY The Compliance Auditor is well versed in healthcare regulations, policies, and procedures, and serves as a protector of revenue for the Munson Healthcare System (Munson) through the completion of formal audits and the provision of various advisory/consultative services. These audits include ...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
SUMMARYThe Compliance Auditor is well versed in healthcare regulations, policies, and procedures, and serves as a protector of revenue for the Munson Healthcare System (Munson) through the completion of formal audits and the provision of various advisory/consultative services. These audits include m...
The Senior Auditor is responsible for performing individual internal audit projects, as part of the total internal audit plan. This responsibility includes developing internal audit scope, performing internal audit procedures, and preparing internal audit reports reflecting the results of the work p...
Purpose Statement / Position Summary Under the direction of the Coding Compliance Manager, the Coding Compliance Auditor/Educator will play a key role in reviewing and analyzing post claim data for accuracy and compliance with federal and state coding guidelines and regulations. The Coding Complianc...
Company DescriptionEurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to t...
ARE YOU A CURRENT US FOODS EMPLOYEE? PLEASE APPLY DIRECTLY THROUGH OUR INTERNAL WORKDAY CAREER SITE. Join Our Community of Food People! The Staff Auditor II will participate in meeting the department objectives including 1) ensuring a strong control environment to protect the company, employees and ...
Remote Clinical Research Associate Location Austin, TX Type Direct Hire Salary $1 - $2 / yr ID BN38-2698383 Posted Aug 18, 2021 Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitor...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Companys clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator s...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator s...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator s...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
$1 to $2 Per Year Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progre...
The Remote (Work from Home) Inpatient Coding Auditor performs inpatient encounter audits and evaluates compliance related activities and services provided by the BayCare Health System HIM Coding Department. Interacts directly with coders, clinical personnel including Clinical documentation specialis...
SUMMARY: The Senior Specialist, Regulatory Affairs provides project representation and input to projects awarded to WCT for all stages of the drug development cycle. RESPONSIBILITIES: Liaise with the Regulatory Affairs Manager/Regulatory Affairs Director to plan, organise, compile progres...
JOB SUMMARY We are looking for an Azure/Google Cloud (GCP) architect to join our growing cloud platform team in designing and developing solutions to support our clinical research teams in Azure/GCP. As a member of the cloud platform team, you will collaborate with other cloud architects an...
Piper Companies is currently seeking a Remote Senior Clinical Trial Manager work for a growing and innovative Oncology Cell Therapy company. Responsibilities of the Senior Clinical Study Manager ·Act as primary contact for site personnel for study related questions, and work directly with...
Job Overview: Study Start Up Specialist Remote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this rol...
Job Overview: Study Start Up Specialist Remote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this rol...
Job Overview: Study Start Up SpecialistRemote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this role you will be...
Job Overview: Study Start Up Specialist Remote - USA based We are seeking a Study Start Up Specialist to be responsible for activities related to study start up and ongoing study document management and act as point of contact for local study teams and external stakeholders. In this rol...