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ScribeAmerica, QueueLogix, CareThrough and SoundLines collectively meet the full range of increasingly complex healthcare data and documentation needs, improving clinical outcomes through highly-skilled clerical support.
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As a Dental Hygienist , you’ll be recognized as an elite clinical provider and patient advocate. Excellent working knowledge of dentistry, dental hygiene procedures, dental patient screening and medical history documentation.
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Live QA – To Assist with OASIS Documentation. Acts as Case Manager when assigned by Clinical Supervisor and assumes responsibility to coordinate patient care for assigned caseload. Daily Pay (Work today.
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Experience in a direct patient care environment preferred i.e. EMT, scribe, clinical technician in hospital, medical assistant in a doctors office. Provide scribe services in an Emergency Department at the direction of a Physician or Advanced Practice Provider (Nurse Provider or Physician Assistant) allowing the provider to spend more time with the patient, work more productively, and produce accurate and thorough documentation in real time.
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Scan all registration and clinical documentation into the system and maintain all medical records. Emerus' leading national health system partners include Allegheny Health Network, Ascension, Baptist Health System, Baylor, Scott & White Health, Dignity Health St. Rose Dominican, The Hospitals of Providence, INTEGRIS and MultiCare.
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SHIFT: Swing shift (1p-1a) - WEEKENDS - Every Saturday and Sunday. Maintain log of all patients, payments received, transfers and hospital admissions. 2 years patient registration and insurance verification experience in a health care setting, required.
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As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. As a Bio-Rad QC Specialist , you will support the testing and documentation needs of the Quality Control Department during the manufacture and release of Bio-Rad control products.
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Review pre-bill cases simultaneously with a physician during each work shift excluding breaks and meetings to analyze and validate diagnosis and procedure codes for inpatient services via coding compliance and clinical knowledge to support accurate DRG assignment.
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Prepare clinical review documentation for review by a MedOne Clinical Pharmacist. Update Clinical Authorization Criteria and Clinical Review Request Forms under the direction of a Clinical Pharmacist.
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Plans, develops, implements, and monitors appropriate provision, documentation, billing of clinical services, and customer relations. The Director of Rehabilitation is responsible for the overall clinical quality, integrity, service excellence, and financial viability of rehabilitation programs within designated geography to ensure customer and company expectations are met.
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The pre-employment physical for positions in clinical areas, laboratories, working with research subjects, or involving community contact requires documentation of immune status against Rubella (German measles), Rubeola (Measles), Mumps, Varicella (chickenpox), Hepatitis B and documentation of having received the Tdap (Tetanus, diphtheria, pertussis) vaccination.
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This role functions at an intermediate level, with responsibility for independent management of simple to moderately complex grants/contracts, including those from NIH, NSF, DOD and NASA. These grants, contracts and awards may involve detailed budgets, subawards and special instructions in RFA, career awards, training awards, multi-project grants, complex Foundation grants, subawards from other institutions on their federal pass-through grants and pharmaceutical company clinical trials.
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This may include documentation of having two (2) MMR vaccines; two (2) Varicella vaccines; or antibody status to these diseases from laboratory testing. These grants, contracts and awards may involve detailed budgets, subawards, pharmaceutical company clinical trials and private sponsors.
$51,210 - $70,480 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Ensure documentation and management of clinical study data is in accordance with regulations. Study documentation production and maintenance, data processing, data review. Knowledge of clinical research including regulatory requirement GCP/ICH Data Quality.
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Manages the direction, planning, execution, and interpretation of all the data management activities related to clinical trials/research (Phase I-IV), including participating in defining corporate practices required for handling the data.
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