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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.
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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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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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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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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 yearFull-timeExpandApply NowActive JobUpdated Today - 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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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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As part of the r, patients are able to receive the world renown treatments, including clinical trials and immunotherapy, of Johns Hopkins Medicine without leaving the region. The Clinical Coordinator is responsible for the day-to-day operations to ensure the Radiation Oncology Clinic runs smoothly.
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We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida.
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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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Reporting to a Clinical Trials Research Nurse Manager, the Clinical Research Nurse will participate throughout the entire clinical trials study process. You will be assisting with the development, implementation, and evaluation of clinical trials for research by pharmaceutical companies, device manufacturers, collaborating institutions, cooperative groups, and internal investigator-initiated studies.
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Serves as protocol liaison to community-based physicians regarding patient referrals for clinical trials in coordination with the ACTU Study Coordinator. Ability to learn the clinical trials and/or grants process.
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If Associates Degree, must have minimum 6 years of work experience) Bonus points if: Experience designing Fund Accounting, Clinical Trials, Labor Costing, Effort Certification, and Pre-Award business processes within an Enterprise Resource Planning platform Experience working within hospital research/grants administration Proficiency in multiple business processes: (PTP, OTC, GL, FA, Budgeting, Cash Management, etc.
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Sr. Financial Analyst or budget preparation, performance of Medicare Coverage Analysis ( MCA ), and negotiation for all industry supported clinical trials and clinical research. Maintains contract templates and site-specific files and databases, and has responsibility for updating the GW OCR contracting manual and relevant SOPs, performs quality control and arranges execution of clinical trial agreements (CTAs) as well as archival of documents into repositories and capture the completion dates and status updates in OnCore Clinical Trials Management System ( CTMS.
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Assist Clinical Scientist, Study Responsible Scientist (SRS), &/or Study Responsible Physician (SRP) in various clinical research assigned Immunology Development clinical trials.
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clinical trials jobs in Annandale, VA
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