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With 15+ years of experience in this space, our teams have supported 1000s of clinical trials, 100s of EDC builds for a multitude of Sponsors/CROs. With a long-standing alliance with Medidata (now Dassault Systems), the leading EDC platform solution provider, we have been successfully implementing Medidata’s best-of-the-breed products to help execute very complex mega-trials for our premium customers.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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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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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.
Full-timeRemoteExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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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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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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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.
$10,000 a yearExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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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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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.
$67,000 - $90,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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.
$10,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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Act as a clinical research pharmacist consultant by collaborating with domestic and international clinical research networks to develop and implement clinical trials, direct start-up activities, coordinate clinical site preparation/renovation, assess factors that may significantly affect a site’s clinical research and pharmacy capacity/operations, and devise solutions and/or approaches to mitigate potential issues.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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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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At least 2 years of prior experience acting as a lead data manager in oncology clinical trials. Associate's degree in the health sciences disciplines or related field of study and a minimum of 8 years of experience in the data management of clinical trials.
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The Director must understand the entire preclinical and early clinical product development pipeline including product optimization, preclinical scale-up, and manufacture and toxicology, regulatory affairs, and early human clinical trials.
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Perform integrative analyses of multi-omics data from clinical trials and research cohorts, including genomics, transcriptomics, proteomics, and imaging, to identify biomarkers related to treatment mechanism and response, and potential therapeutic targets.
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clinical trials jobs in Bethesda, MD
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