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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.
$42,953 - $77,315 a yearExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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The Community Practice Clinical Data Coordinator at Trial Library will play an integral part in expanding access to cancer clinical trials by pioneering pre-screening efforts in community oncology settings.
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The Associate will be a member of the Biorepository and Biomarker Core and be involved in clinical trials, translational research, and basic science research. · Clinical data extraction for biomedical research and clinical trials.
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Assist with the coordination of study start-up for Network clinical trials; work with the UCLA Study Teams, IRB and Pharmaceutical sponsors and CROs for network site participation. Assist with clinical trials regarding Network study start-up requirements and regulatory processes.
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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 primary responsibility of the Research Nurse is to manage RN responsibilities in the conduct of clinical trials. The Research Nurse I provides direct patient care for clinical trials subjects.
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Reporting to the Clinical Research Manager of Blood & Marrow Transplantation and Cell Therapy (BMT-CT), the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to to manage data, enroll and follow patients on trial, and assist with regulatory and financial requirements of the trials.
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During the one-year fellowship, the F.A.S.T. fellow will learn about clinical trial design, including novel clinical trials for rare genetic pediatric NDDs including N-of-1 trials, development of specialized programs for clinical management of these conditions with accommodation of experimental treatments, and new outcome measure and biomarker development for these populations.
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Meets requirements of Clinical Trials Senior Chemotherapy Nurse 30% Abides by requirements in accordance with the Oncology Nursing Society’s Manual for Clinical Trials Nursing.
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Interacts with Levine Childrens Hospital Pediatric Blood and Marrow Transplant Program Works with Clinical Trials Office staff on clinical trials involving cell therapy Maintains cell dose and engraftment data Provides adequate systems to manage, track and securely store product/patient files to meet or exceed institutional and external regulatory guidelines (FDA, FACT, and CAP.
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As a part of Clinical Trials Scientific Affairs, the Principal Scientist will support testing, method development and validation. Collaborate with Research & Development, Scientific Affairs, and Laboratory staff in any way applicable to support Clinical Trials.
$115,000 - $130,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Processes patient specimens for Fate’s clinical trials to perform biomarker testing using multi-parameter flow cytometry and other cellular immunology assays. Fate Therapeutics is seeking a motivated individual skilled in immunology and/or cell biology to join our Clinical Translation team in support of the company’s clinical trials utilizing off-the-shelf, iPSC derived immunotherapies.
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Job Req ID: 112971 Clinical Research Monitor The Department of Neurology is seeking a who will take the lead on compliance monitoring of predominantly large, multi-centered, clinical trials in keeping with established BIOS Clinical Trials Coordinating Center (CTCC) policies and procedures and GCP. The CRM will ensure quality, accuracy and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials through utilization of a risk-based, remote monitoring approach.
$55,200 - $96,600 a year depends on experienceFull-timeExpandUpdated 29 days ago - UpvoteDownvoteShare Job
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Experience with conduct of clinical research with pharmaceutical/device clinical trials and/or observational or social behavioral and/or public health research. 5 - 8 years relevant experience working as a clinical research coordinator role (project manager, research assistant, study coordinator, etc.
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Position RN Clinical Research Cancer - DAY SHIFT - Hematology Oncology Clinical Trials. Under the direction of the Cancer Center Clinical Trials Office Administrative Director, the Clinical Research Cancer nurse will lead day-to-day operations of clinical research studies conducted by principal investigator(s) at Penn State Cancer Institute Clinical Trials Office.
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clinical trials jobs Title: regional Company: Florida Cancer Specialists
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