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Medical Center: UH: Clinical Lab (Full-Time, Evening Shift) - Job Summary: The Clinical Lab Scientist 1, under general supervision, operates specialized instruments to conduct clinical lab tests and analyze data from results, to assist physicians with diagnosing medical conditions.
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You will lead internal peptide therapeutics development projects from drug discovery to Phase-2 clinical trials. PhD, MD, DO, DVM, or equivalent in Chemistry, Biochemistry, Medicinal Chemistry, or related field.
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Our team is actively involved in research projects and clinical trials, collaborating with Harvard Medical School, Duke University and Eli Lilly. The ACC National Cardiovascular Data Registrys ("NCDR") partner, Veradigm Cardiology Registry (formerly PINNACLE Registry), recognized HIETs contribution in providing registry data used to improve processes and procedures that establish high quality cardiovascular care.
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We also maintain a dynamic portfolio of industry-related oncology, hematology, and sickle cell clinical trials. The Division is an active participant in clinical trials through the Children’s Oncology Group, Beat Childhood Cancer, and the Pediatric Transplantation & Cellular Therapy Consortium.
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Leverage clinical and data domain knowledge to build data extract, delivery, and transformation processes to meet user requirements. Understanding of data warehousing concepts and experience with data warehousing solutions (e.g., Snowflake, Redshift, BigQuery.
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Located just 30 minutes from the beach, TidalHealth offers the widest array of specialty and subspecialty services such as neurosurgery, cardiothoracic surgery, joint replacement, emergency/trauma care, comprehensive cancer care, wound care and clinical trials and research.
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Work with the start-up team, CTMS and UW Clinical Trials Office (CTO) to review billing calendars, Medicare Coverage Analysis (MCA), and financial entries and bill routing. Knowledge of the Medicare Clinical Trials Policy and other federal, state, and institutional clinical research regulations.
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PhaseForward Inform, Oracle Clinical and/or other clinical data management software desirable;General software skills: MS Access, MS Word, MS Excel, MS Project, Visio, familiarity with medical coding dictionaries, especially MedDRA and WHODRUG.Experience applying best practices in clinical data management programming in the clinical trial environment, including requirements definition and QC plansKnowledge of GCP and other regulations.
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Responsibilities The Trauma Registrar collects, abstracts and enters clinical data for all trauma patients admitted to or evaluated by the trauma service. When it comes to trauma data management, it’s about professionals who can review abstract and validate data for the Trauma Registry, submit data to state and regulatory agencies and work as a liaison between performance improvement functions and the registry.
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Key responsibilities include performing ophthalmic examinations according to research protocols, coordinating research studies and trials, performing protocol-related procedures under the guidance of the Clinical Research Coordinator and Manager, and assisting with research study documentation and IRB submissions.
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Required Experience: Degree in epidemiology, biostatistics, data science, clinical informatics, public health, or related fields. The Data Scientist will collaborate closely with product, operations, engineering, data science, and clinicians to provide best in class analysis of oncology care pathways and contribute to technical product requirements with supervision from senior scientists.
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Ensures all appropriate CMC regulatory aspects for clinical trials/product release are in place, to avoid clinical holds and/or to ensure continuity of market supply. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology.
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Previous clinical laboratory experience as a Medical Laboratory Technician, Medical Technology, Clinical Laboratory Scientist or Medical Laboratory Scientist within a clinical laboratory.
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This research nurse position will work collaboratively with physicians in identifying and managing patients on NCI and pharmaceutical sponsored clinical trials. MMCORC provides the opportunity for patients and physicians to have access to National Cancer Institute (NCI) and pharmaceutical sponsored clinical trials for all types of adult cancer.
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Our team of nationally renowned doctors, specialists, surgeons, genetic counselors, nurses and caregivers are backed by the latest in drug discovery, clinical trials, research and advanced treatments.
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clinical trials data jobs Title: operations Company: Boston Pharmaceuticals
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