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The Senior Specialist serves as leader within the Office of Ethics and Compliance (OEC) and serves as a resource to the greater university community; coordinates oversight and compliance activities with other units across UCSF; and communicates compliance obligations while assisting faculty and staff in translating compliance requirements and expectations into their daily work.
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Master’s or Doctorate in Nursing (Nurse Practitioner, Clinical Nurse Specialist, Certified Registered Nurse Anesthetist and Certified Nurse Midwife); Master’s or Doctorate in Science (Physician Assistant.
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We currently have a position for a Research Associate located at Walter Reed Army Institute of Research in Silver Spring, MD. This position will be supporting Shigella vaccine development.
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You will also contribute significantly to our research and clinical development efforts as a core member of our research governance committees, and function as a core team member of our CSO Leadership Team and CSO Strategy Team to provide scientific input for translational and clinical biomarker strategy of all our pipelines.
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Working with Clinical Research team and key personnel including the Executive VP of Clinical Research, this highly skilled and team-oriented Medical Director will be a physician and will have subspecialty training in Nephrology or Infectious Disease or Rheumatology and have at least 1.5 years of clinical research and development experience.
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Other content knowledge that will support CEA’s work includes land preservation, sustainable agriculture, freshwater management, forestry, environmental justice, and/or air quality. Preferred Experience Proficiency in qualitative research methods (e.g., interviews, expert consultation, case studies.
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Minimum of 10 years of working in clinical research and drug development in the pharmaceutical industry (and/or Contract Research Organizations) with specific experience with TMF, clinical documentation and/or records & information management.
$205,000 - $260,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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UCSF Department of Ophthalmology is a nationwide leader in clinical care, medical training, and research. Dr. Shan is a glaucoma specialist and a medical engineer whose research aims to leverage computational innovations such as artificial intelligence (AI) to broaden access to glaucoma care and vision-saving therapies.
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CERTIFICATION & LICENSURE: Certified Clinical Documentation Specialist (CCDS) or Certified Documentation Improvement Practitioner (CDIP)Certified Coding Specialist (CCS) or Certified Professional Coder (CPC)SKILLS AND KNOWLEDGE:Knowledge of Pathophysiology and Disease Processes sufficient to pass the clinical pre-employment test at a rate of 85% or better is required for new hires.
$63.74 - $95.6 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our QSP & PBPK team has established expertise, impact, and tools, and we are looking for a highly motivated scientist to develop and apply Quantitative Systems Pharmacology (QSP) models with a primary focus on hematology, oncology, and cell therapy applications to primarily impact clinical development.
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Extensive knowledge of regulatory standards (e.g. ICH-E3, ICH-E6, eCTD) and industry-wide standards in clinical document management and records management (e.g. DIA TMF reference model) They are responsible for TMF process development and implementation and will ensure processes are designed to support the business and TMF needs across the entire Research & Development (R&D) organization of Eidos and BridgeBio. Implementing appropriate controls, standards, and metrics to ensure oversight and compliance in the short and long term.
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The Clinical Quality Measurement team manages HEDIS annual submissions and other quality measure submissions to CMS, NCQA, DHCS and other governing bodies. In this role You will support corporate and departmental strategies and goals for the annual HEDIS submission process and effectively apply business knowledge and technical expertise to support the business initiatives to report clinical quality of care received by members.
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1-3 years of laboratory technician, or research experience, especially in supporting more experienced engineers/scientists in an industrial setting. At Shennon Bio, we are dedicated to advancing immunology research and making a positive impact on healthcare.
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The HBC Quality Management Analyst will also work closely with the Quality Nurse Manager and with other managers from the Infusion, Apheresis, Inpatient and Outpatient Clinical Units, and the Blood and Marrow Transplant Lab on projects designed to improve effectiveness or efficiency in several quality initiatives, data management, and efficiency in quality operations.
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These services consist of several functional areas housed within the HDFCCC, including the DSMC, Clinical Research Support Office (CRSO), Clinical Research Network Office (CRNO) and the Protocol Review and Monitoring Committee (PRMC), with oversight from the Cancer Center Clinical Research Oversight Committee (CCCROC.
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clinical research quality specialist jobs Title: quality specialist Company: Quest Diagnostics in San Francisco, CA
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