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The person will support Infectious Disease Physician Investigators in clinical research ranging from observational trials to investigational drug/product trials, including investigator-initiated, government funded, and industry-sponsored trials.
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The Clinical Research Coordinator assists the clinical trials process by registering hematology, oncology, and bone marrow transplant patients for clinical studies, assessing eligibility criteria, maintaining current protocol packets and assuring that all quality assurance measures are maintained within the protocol/study.
$39,300 - $64,349 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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This work is supported by the Cancer Center Clinical Trials Unit, a new cGMP and TCT laboratory, fully characterized tumor samples repository and new state-of-the-art Medical Center opened in 2021, all on the Medical School campus.
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Onsite) FUNCTION: Clinical Operations – Biomarker and Bioanalytical Operations Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Company therapeutic areas.
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The department is active in basic radiation biology, and physics research as well as clinical research with an emphasis on investigator-initiated trials. In addition to accredited radiation oncology residency, medical physics residency, and radiation therapy technology programs, the department has active clinical programs in brachytherapy, pediatric radiotherapy, total skin electron irradiation, total body irradiation, and Gamma Knife radiosurgery.
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The Knight Cardiovascular Institute Senior Clinical Research Coordinator is responsible for various duties related to clinical trials. The Senior clinical research coordinator is also the primary liaison for patients receiving care on a clinical trial and is responsible for the triage of patient needs.
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The Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The coordinator will work on 10-15 clinical trials primarily within sickle cell disease.
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The Rater is responsible for the organization, administration, management, and efficient execution of clinical ratings associated with clinical trials. Manage aspects of the study related to ratings with the rater training representative, study sponsor, Site Director, and Principal Investigator to ensure compliance with protocol requirements.
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The range of these research projects are extensive and comprehensive, extending from biomarker/natural history studies to Investigator Initiated studies to Industry clinical trials (Phases 1-3.
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Complies with GCP's (Good Clinical Practice) guidelines and follows all FDA regulations with regard to clinical trials. 5.1 Responsible for processing of contract in conjunction with Bridgeport Hospital legal counsel, Sponsor, and Principal Investigator.
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Carbon Health is looking for an excellent full-time Primary Care Physician with clinical research experience as a Principal Investigator to join a growing community of healthcare providers to deliver compassionate, evidence-based urgent care and conduct clinical trials in infectious disease and indications related to general medicine, including vaccine research and cardiometabolic health.
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This position offers postdocs the opportunity to gain exposure to design, conduct, and analysis of complex clinical trials; to develop expertise in digital health, violence prevention, communication, and adolescent health; and to expand their capacity for team science and successful grant writing in the fields of emergency medicine, behavioral health, and violence prevention.
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Coordinate and facilitate the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated. The position will work closely with the members of the clinical research team to develop effective tools for close monitor and reporting of trials accrual and coordinate the timely study activation and submission of protocol amendments.
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Statistical Programmer, clinical trials, SAS. Provide Statistical Programming support in producing or verifying SAS scripts and outputs for Analysis Files, Tables, Listings, Figures, and any other form of Clinical Trials.
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Department: MED-Clinical Trials Unit Salary/Grade: EXS/8 Job Summary: Under general supervision and according to standard practice or general instruction, directly supports the research initiatives of the Bluhm Cardiovascular Institute Clinical Trials Unit. Collaborates with the physicians and clinical team in implementing investigator-initiated, industry-sponsored, as well as federally funded protocols, including multi-center clinical trials.
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