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Knowledge of and ability to accurately follow all SOPs associated with a GLP study, including required by study protocol and GLP documentation procedures. Knowledge of techniques and ability to collect samples for laboratory study.
$24 - $28.31 an hourFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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This coordinator will participate in all regulatory aspects of clinical trials from study acquisition, including study start up and initiation, maintenance of projects through to study closure.
$27ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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You will be responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP.
$32.65 an hourExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Participate in study-related meetings, including investigator meetings, protocol training sessions, and data review meetings. Lead study design, protocol development, and implementation in collaboration with cross-functional teams.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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As a Clinical Research Coordinator I, you will work independently providing study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
$23.39 - $39.76 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Oversee the development and finalization of clinical operational plans (eg Monitoring Plan, TMF Plan, Protocol Deviation Plan) case report forms, informed consent documents, study specific forms, study training and reference materials.
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Fills out protocol specific data management forms, i.e., Study Parameter Worksheets, Toxicity Assessment forms, etc. Conducts ongoing assessment of protocol deviations and violations during patients’ time on study.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The CRC is responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The incumbent is responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP.
ExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Perform data review of both integrated data to identify study trends and patient centric data from ongoing and completed clinical study (ies) to ensure compliance with study protocol and GCPs. Will work with Clinical Operations to implement corrective actions as needed for noncompliance.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience.
ExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The CDC is also responsible for regulatory compliance for each study, patient scheduling and support, and ensuring protocol procedures are completed accurately, safely, and in a timely manner.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Data extraction from source documents and assist CRC with query resolution Basic knowledge of clinical trials and medical terminology In-depth understanding of departmental, protocol, and study-specific procedures Proficiency in MS Windows and Office applications (Access, Outlook, Excel, Word) Excellent interpersonal and communication skills Strong attention to detail and ability to work independently.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Ensure studies are carried out according to the study protocol, SOPs, and ICH/GCP regulations and study-specific manuals and procedures. · Oversee the performance of CROs and third-party vendors, including co-monitoring, to ensure compliance with study protocol and in accordance with scope of work; identify areas of concern and escalate to Clinical Operations Managers.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Prepare specimen aliquots as per protocol definition including serum, plasma, urine, feces, and other biofluids depending on study protocol. Assist project managers in preparing sites for collection including kit assembly, shipping, and study binder preparation.
Full-timeExpandApply NowActive JobUpdated 1 month ago
protocol study jobs in Los Angeles, CA
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