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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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Provides direct oversight of: Sr. Financial Analyst or budget preparation, performance of Medicare Coverage Analysis (MCA), and negotiation for all industry supported clinical trials and clinical research.
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May represent the county in other civil and administrative actions such as county or state code enforcement actions, child support cases, involuntary commitment and treatment hearings and trials, and other civil actions brought on behalf of or against the county in local, state, or federal courts.
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Minimum of five (5) years of progressive experience in managing clinical trials/clinical research sites and/or monitoring clinical trials. Provide leadership for planning, organizing, and conducting site visits or reverse site visits as appropriate to clinical trials units/clinical research sites to effectively fulfill site management responsibilities.
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The Clinical Research Coordinator 2 (CRC2) manages and coordinates 7 out of approximately 55 ongoing clinical trials, Phases I-IV, in the Department of Neurology, primarily in the neuromuscular disease.
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Provides legal representation to prosecute a broad range of difficult and complex criminal cases in District, Juvenile, or Superior Court including bench and jury trials of felonies, gross misdemeanors, misdemeanors and violations that occur in Mason County.
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Support clinical trial-related activities: provide support and oversight to staff with regards to safety in clinical trials; review and provide input and support on clinical trial-related documents (e.g. study protocols, statistical analysis plans, safety-related data collection forms, and the design of tables, figures, and listings for clinical trial safety data); review of adverse events or serious adverse events from clinical trials; and participate in study team meetings.
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Working knowledge of clinical trials contracting and budgeting, including understanding of Medicare Coverage Analysis (MCA) and clinical trials billing compliance, both industry and non-industry.
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Suburban Hospital, part of the Johns Hopkins Health System, offers direct access to world class, innovative and ground breaking care provided by teams of specialists in medical oncology, radiation oncology and surgical oncology, with access to advanced treatments through Johns Hopkins clinical trials.
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Develop novel methodologies for analyzing immunological and pharmacokinetic data from both vaccine and monoclonal antibody clinical trials. Responsibilities Provide accountability for the scientific deliverables and contributions of the Vaccine Research Center’s (VRC) Translational Science Team. Oversee essential team functions, ensuring that: All scientific objectives of VRC clinical trials are met; Clinical trial data is accurately analyzed and project timelines established by VRC leadership are met.
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Our work ranges from basic to translational and clinical, and our clinical trials are conducted in the NIH Clinical Center, the world’s largest hospital dedicated to clinical research that offers a robust infrastructure to support CCR’s patients on an estimated 250 open studies.
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The Clinical Research Coordinator 2 (CRC2) is responsible for managing and coordinating 7 out of approximately 55 ongoing clinical trials, Phases I-IV, in the Dept. of Neurology, primarily in the disease states of Stroke, Multiple Sclerosis (MS), Stroke, and neuromuscular disease.
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This position manages the research related care of these patients, assists in project initiation, facilitates patient enrollment, encourages patient retention in trials, reports to sponsors on progress/status, and coordinates study participation with other clinical care plans.
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JOB SUMMARYThe Research RN, NCHRI works directly with the physician in accurately and professionally executing all clinical research projects in an acute care/inpatient setting (ED, Cath Lab, ICU, EP lab, Step down and OR) as well as the ambulatory and ancillary areas.
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CfOR scientists partner with internal team members and industry experts to design, conduct, interpret and publish observational research that informs decision-making from the early development of a molecule to the design of clinical trials and the safety and efficacy of Amgen medicines.
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trials job in Washington, DC
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