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RDI is seeking a Senior Clinical Associate to ensure our clinical trials are completed on-time, according to the protocol, and keeping our clients and sites informed throughout the process.
$1 - $120,000 a yearExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Overview: Position Summary: As a member of the Bone and Soft Tissue Tumors team (BSTT), the Clinical Research Coordinator II will be responsible for managing multiple clinical trials of phases I through III in accordance with federal and local regulations.
$27ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Assist Clinical Scientist, Study Responsible Scientist (SRS), &/or Study Responsible Physician (SRP) in various clinical research assigned Immunology Development clinical trials.
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Carbon Health is looking for a General Medicine 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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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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Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.
$32.65 - $52.63 an hourFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Responsibilities:Coordinate and oversee all aspects of clinical trials as an IP designee. This role is critical for the safe and effective management of investigational drugs used in our clinical trials.
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Our company is looking for qualified candidates to participate in paid national and local focus groups, clinical trials, and also market research studies. This is an excellent opportunity to supplement your income if you are a data entry clerk or anyone seeking a flexible part-time remote work from home job.
TemporaryRemoteExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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OneOncology’s non-exclusive clinical trial site management subsidiary, OneR, delivers complex, multi-center clinical trials to affiliated practices. Ability to Enroll Patients in Clinical Trials.
$375,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Join this world-class team providing highly-specialized care, up-to-the-minute research and innovative clinical trials. As part of Keck Medicine of USC, USC Verdugo Hills Hospital is the only community hospital in the Foothills area of Los Angeles backed by an academic medical center.
Full-timeExpandUpdated 3 days ago - UpvoteDownvoteShare Job
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Exciting opportunity to work as a coordinator in an ongoing cohort study and new clinical trials at the Center for Cardiac Arrest Prevention (CCAP). The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
$28.3 - $48.11 an hourFull-timeExpandUpdated 20 days ago - UpvoteDownvoteShare Job
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Description The David Geffen School of Medicine, Department of Urology is seeking to hire a Full Time Senior Study Coordinator for pharmaceutical and industry sponsored, investigator initiated, and NIH-sponsored clinical trials.
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Provide clinical support for ongoing and upcoming clinical trials related to Orphan Drugs and Inherited Enzyme Disorders. Advanced degree in a scientific/clinical discipline required - Pharm D, PhD, MD.
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A joint venture of IQVIA (formerly QuintilesIMS) and Quest Diagnostics, Q2 Solutions combines the best of each parent organizations clinical trials laboratory services capabilities to fulfill its mission of treating each sample as if a life depends on it.
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This role is an opportunity for an experienced Clinical Operations Professional with technical expertise supporting Phase I-III clinical trials in an industry setting and a strong knowledge of clinical operations, Good Clinical Practice (GCP), and U.S. Food and Drug Administration (FDA) regulatory requirements.
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clinical trials jobs in Los Angeles, CA
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