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How you will make an impact:Maintain schedules for employee visits and accurate information in employee medical recordsPerform front desk receptionist responsibilities to include data entry, assisting customers as they enter Employee Health, filing and retrieving medical charts, and answering phones.
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Closely follow medical developments within assigned areas, including cell therapy for oncology, and disseminate new information within Clinical Team and wider organization, to transform trends and emerging data into agile clinical plans.
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Use Western blot/ELISA, molecular and system biology techniques, nucleic acid and protein extractions with quality check, PCR, microbiome, metabolomics, pyrosequencing, statistics and data analysis and visualizations.
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Westat is seeking Medical Records Abstractors or individuals with some experience with medical records or health insurance records coding, quality control or review, or similar skills and/or experience to work on-site at our Rockville campus on a data collection effort to abstract specific data items from hospital data.
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The Auditor reviews medical records to determine data quality and accuracy of coding, billing, and documentation related to DRGs, APCs, CPTs, HCPCS Level II code and modifier assignments, ICD diagnosis and procedure coding according to regulatory requirements.
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Job Type Full-timeDescriptionJob Summary: Responsible day-to-day administrative and general office duties including word processing, filing, faxing, and data entry. Experience: One year of experience in customer service or reception, preferably in a medical office setting.
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Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.
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Leidos National Security Sector is seeking a fully cleared Wellness Medical Administrator who is seeking a rewarding and challenging opportunity for an Intelligence Community (IC) customer in Northern Virginia.
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Gather feedback, data, or information during routine activities that can help the Company better comprehend the medical or scientific needs, priorities, or concerns of healthcare practitioners (HCPs) and/or patients.
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The Medical Science Liaison (MSL) is a field-facing representative of US Medical Affairs with a primary responsibility of engaging in the exchange of scientific data and other medical and/or scientific information with external customers (Health Care Providers, researchers, professional organization leadership, and population-based decision makers) in the areas of Eisai’s interest.
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Utilize Accreditation Council for Graduate Medical Education (ACGME) Web Accreditation Data System (ADS) to review changes or updates in the GME program(s) policies and/or procedures. Provide comprehensive program management, expert assistance, advice, direction, implementation of quality improvement processes and oversight of Graduate Medical Education (GME) programs.
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Processes data and enhances digital images using advanced computer technology. Provides images, data analysis, and patient information to the physician for diagnostic interpretation. BASIC LIFE SUPPORT - American Heart Association, Certified Nuclear Medicine Technologist - Nuclear Medicine Technology Certification Board, Medical Radiation Technologist Mississippi - Mississippi State Department of Health, Radiologic Technologist Arkansas - Arkansas Department of Health, Registered Radiologic Technologist - American Registry of Radiologic Technologists.
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Reviews sample run data and quality control data and ensures all regulatory compliance standards are met while following established SOPs. Ensures proper entry of specimen data and testing results into databases or the laboratory information management system (LIMS.
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Serves as technical expert and functional project manager for implementation of national patient safety goals (NPSG) and other initiatives, identified through adverse event reporting and data analysis.
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You will have a proficiency in the drug development process, particularly early phase clinical trials, protocol writing and study conduct, data review and reconciliation. Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems, and final reports.
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data job Title: medical in Rockville, MD
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