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The PACS research program is funded through 11 NIH awards in addition to awards from the Cystic Fibrosis Foundation, other federal sources and foundations, and many industry-funded clinical trials.
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Supports IRB approved clinical research/trials though a variety of activities including but not limited to: obtaining consent; ordering diagnostic tests; recording laboratory and diagnostic results; administering therapeutic interventions; and documenting and reporting patient outcomes including toxicities or adverse events.
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This includes driving and supporting project design, implementation, and programmatic innovation (including impact of climate change) to understand disease etiology and vectors, develop diagnostics, manage clinical trials, and maximize genomic applications.
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This role's primary focus will be providing clinical education to current and potential customers, provide internal training to hospital sales reps., set up trials and conversions, and support industry trade shows.
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A unique, yet limited aspect of our unit is our contractual agreement with the National Institutes of Health (NIH) to support the care of our patients enrolled in clinical trials. Articulates application of Synergy model for care in clinical practice.
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Serves as a clinical expert and education consultant to nursing, members of the healthcare team and to the larger community. Performs approved therapeutic or diagnostic procedures based upon patients clinical status and documents procedures in accordance with hospital requirements, including obtaining arterial, venous, and capillary blood samples, urine samples, sputum samples and cultures; performing cardiac output measurements, other hemodynamic measurements and EKGs; assisting with the performance of radiographic studies; assisting physician with diagnostic and therapeutic procedures; etc.
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Lead biomarker and pharmacokinetic planning, definition, and implementation, overseeing sample collection for early and late-phase clinical trials. Extensive oncology experience, including proficiency in target/disease biology, preclinical, and clinical development.
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Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and SOPs. Implement and coordinate assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.
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The Advanced Cell Therapy GMP Scientist will also make preliminary selections and adaptations of scientific alternatives requiring the exercise of judgment be involved in the rapidly growing multiple clinical trials within the cell therapy areas.
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Seeking a highly motivated and detail-oriented Clinical Technology Program Coordinator. Bachelor’s Degree in a relevant field (Biology, Clinical Research, Health Sciences, etc.) Project Coordinator III (Clinical Technology) for a prominent client of ours.
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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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At Science 37 Atlanta, Georgia - Remote Science 37 is accelerating the research and development of breakthrough biomedical treatments by bringing clinical trials to patients' homes. Backed by venture investors such as Glynn Capital, Google Ventures, Redmile Group, dRx Capital and Lux Capital, we are revolutionizing the clinical trial industry, one patient, at a time.
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Derive novel prognostic and predictive signatures using statistical and machine learning methods to guide patient stratification and biomarker selection in clinical trials. This position will be focused on the bioinformatics collaborations in Oncology clinical trials and will thus play a crucial role in analyzing large-scale genomic and clinical datasets to uncover insights into cancer biology and treatment response.
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Join other professionals revolutionizing efficient and seamless study start-up to advance clinical trials. This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace.
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In addition, we offer our physician partners access to a robust suite of ancillary services, clinical research trials, as well as professional collaboration with a growing team of GI physicians and advanced practice providers.
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clinical trials jobs in Atlanta, GA
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