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Perform medical case review of Serious Adverse Events (SAEs), including review of coding, consistency in assessment, case documentation and patient narrative. Proficiency in MedDRA coding, Microsoft Excel, Word, and PowerPoint; safety database experience preferred; ability to learn new computer systems as they are implemented.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Experience working with system integrators for IVRS, medical coding, eSource, CTMS, eTMF, and other clinical technologies. Vault CDMS combines EDC, coding, data cleaning, and reporting into one application.
$80,000 - $200,000 a yearRemoteExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Experience with basic coding systems such as Grasshopper, Dynamo, Arduino, or Python. Our innovative approach defies gravity by suspending prints within a safe, reusable gel matrix, revolutionizing non-planar printing for cost-effective solutions in medical, apparel, home goods, aviation, marine, and automotive industries.
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In this role, you will collaborate under the guidance of the Lead Data Abstractor, contributing to the extraction and coding of vital information in accordance with the prescribed format, ensuring compliance with the requirements of the designated registry.
Part-timeRemoteExpandUpdated 14 days ago - UpvoteDownvoteShare Job
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Under the guidance of the CRD he/she collaborates with the Coding specialist, Biostatisticians, Data Managers, Global and Regional Study Managers, Feasibility Managers, Pharmacovigilance representative, Medical Writer (e.g. planning and review of narratives) on high quality medical review, as needed.
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The Coding Specialist II reports to the Supervisor/Coding Manager/Senior Coding Manager and is responsible for correct coding of professional services and upholding compliance standards.
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May provide specific subject matter expertise working across all clinical trials, e.g. medical coding, risk-based data quality management, external data management, etc. Data quality surveillance of CRF and external/non-CRF clinical trial data (e.g. Biosample Lab Data, Biomarker Data, Imaging) in collaboration with other Clinical Operations roles, Medical Monitors, Translational Medicine, Clinical Pharmacology, Biostatistics, and other internal and external stakeholders.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Demonstrated proficiency in drug safety databases (e.g., Argus), electronic data capture systems, and coding with MedDRA and WHO Drug dictionary. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Expert knowledge of ADA codes, CPT Codes axiUm expert; MassHealth and Medicare regulations and guidelines, as well as commercial dental/medical insurance coding/billing practices. BA/BS OR Associate's Degree and 1 year experience OR High School Diploma/equivalent & 3 years related experience in dental/medical revenue cycle operations or similar industry business operations.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Applications Coordinator reports directly to an Applications Manager within the Cadence, ADT/Prelude, HIM, Coding, Resolute Hospital Billing, Resolute Professional Billing application teams; s/he is part of a team dedicated to configuring, building, testing and activating the assigned application database.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Perform medical review of ICSRs in Xenon's Global Safety Database including but not limited to case narrative, MedDRA coding, labeling, causality, company comment and queries. Contribute to safety sections of clinical study documents including Study Protocols, Informed Consent Forms (ICF), Statistical Analysis Plans (SAP), Medical Monitoring Plans (MMP), Clinical Study Reports (CSR), IB Reference Safety Information (RSI), Summary of Clinical Safety (SCS), Integrated Clinical Safety (ICS), Publications, Manuscripts, and other relevant documents.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Perform comprehensive inpatient DRG validation reviews to determine accuracy of the DRG billed, based on industry standard coding guidelines and the clinical evidence supplied by the provider in the form of medical records such as physician notes, lab tests, images (x-rays etc.
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Highly competent in clinical data management, various EDC systems, CDASH/CDISC standards and medical coding dictionaries. PhD with 8-12+ years’ experience or MS with 12-15 years’ experience in the pharmaceutical industry or healthcare sector, with joint experience / degree in Computer Science, Medical Informatics or Bioinformatics.
$250,000 - $290,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Experience with medical coding systems (e.g., NDC, ICD-9, HCPCS/CPT, SNOMED CT, LOINC), basic medical terminology, and epidemiologic principles a must. Experience analyzing large administrative healthcare data a must (Medicare/Medicaid, other claims-based or electronic medical records databases.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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This role is key to help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical & Sciences Operations Platform (CSO) and Development Units in company's R&D.
ExpandApply NowActive JobUpdated 9 days ago
medical coding jobs in Roslindale, MA
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