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Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs.
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The trauma performance improvement (PI) / research coordinator works collaboratively with the Trauma Program Manager, Trauma Medical Director, and Trauma Director on clinical and research components of the Trauma Program.
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Collaboration with staff in Biostatistics, Clinical Data Management, and Clinical Research and Global Drug Safety. Support real-time online clinical trial data review.
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Christiana Care Health System is currently seeking a Research Nurse Coordinator with two years of Oncology Clinical experience for our Cancer Research Department at the Helen F. Graham Center & Research Institute in Newark, DE.
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At each of our 12 multidisciplinary disease site centers, patients have a fully dedicated team that include oncologists, surgeons, navigators, and social workers, as well as a clinical research nurse at each MDC to explore avenues for potential cutting-edge treatments in the latest clinical trials.
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Serves as a preceptor and mentor for new or less experienced research nurse coordinators, clinical research associates, and support staff. In this role the Research Nurse Coordinator screens, enrolls, plans, implements, and evaluates protocol-related care of participants and data for assigned research projects.
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The department of Computational Biology is seeking an experienced Bioinformatics Research Scientist to lead the development of bulk and single-cell RNseq-based pipelines for use in our clinical genomics program.
$154,960 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Communicate closely with the sponsor’s Clinical Research Associate (CRA) to facilitate the sponsor monitoring and data maintenance process. The Clinical Research Coordinator (CRC) is responsible for overseeing the day-to-day operations of clinical trials designed to test the safety and effectiveness of new drugs.
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Responsibilities: Conducting all trial visits Completing all study-specific assessments (e.g. vital signs, EKG, blood collection) Processing all samples and shipping to Central Lab Maintaining study source Entering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working autonomously.
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Research experience in statistics and computational genomics, and familiarity with next-generation sequencing data and analysis tools (preferred). Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
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Job Description: The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials.
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Seeks authorization from the Director for any psychology student training, including both clinical and research training. Basic understanding of and skills in teaching and education, clinical supervision, and training and research.
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Keywords: Data Analysis, SQL, Tableau, dashboard, Data Analysis, Data Quality, Data exploration, data visualization, statistical and non-statistical modeling, predictive and prescriptive analytics, analytic programming, database management, master data management, data quality, ETL, storage, processing, cloud computing, healthcare electronic medical record systems, billing systems, imaging systems, ambulatory, acute, post-acute.
$136,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Business Administration, Business Strategy, Clinical Pharmacology, Clinical Research, Collaboration, Communication, Conflict Solving, Data Entry, Drug Development, Enterprise Mindset, Influence, Leadership, Mentoring, Microsoft Office, Oscilloscope, Partnership, Patient Care, Physics, Quality Control, Transactional Analysis.
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Demonstrated ability in the following skill set: Interpretation of technical data specifications Critical thinking Excel spreadsheet use Problem-solving Research Project management EMR and data aggregator software Communication, verbal and written Presentation Skills ESSENTIAL FUNCTIONS Provides administrative support to ensure success of IPA's Medicare Risk Adjustment, HEDIS and CMS STARS initiatives.
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clinical research data jobs Title: records administrator
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