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The regulatory coordinator will integrate information from multiple sources and use specialized regulatory knowledge of the governing clinical research policies to ensure all clinical trials are compliant with applicable federal and institutional regulations.
$6,800 a monthFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Regulatory Coordinator Oncology Clinical Research Unit [CRU] Brain TUMOR CLINICAL Research Program [BTC] Position Description, Occupational Summary Perform regulatory and safety processes for multiple, complex oncology clinical trials and research studies including Investigational Products [IP] for the Duke Cancer Institute’s [DCI] TEAM Clinical Research Program [BTC.
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Manages submissions to the Institutional Review Board (IRB) Performs additional non-clinical clinical research coordinator duties (eg data collection, obtaining informed consent) as necessary.
$58.05 an hourExpandUpdated 2 days ago - UpvoteDownvoteShare Job
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Develop and submit Institutional Review Board [IRB] documents such as consent forms, protocols, and continuing reviews. Preform regulatory and safety processes for multiple, complex oncology clinical trials and research studies including Investigational Products [IP] for the Duke Cancer Institute’s [DCI] Melanoma Clinical Research Program [MEL.
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The position will manage all aspects of study start-up, modification submissions, continuous reporting, and study close-out to the Institutional Review Board (IRB) and any relevant regulatory agencies including, the Institutional Biosafety Committee, the institutional Radiation Safety Committee, and the clinical trial sponsor, funding foundation, or governmental agency.
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Ensures compliance with regulations, including organizing electronic files and/or filing regulatory documents appropriately; prepares and submits Institutional Review Board (IRB) documents (i.e., Informed Consent, advertisement, protocol and protocol summary); prepares regulatory documents for sponsor.
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Independently prepare, develop, and submit Institutional Review Board (IRB), Biosafety, and Research and Development Committee documents such as protocols for initial submissions, protocol amendments, and continuing reviews for both human subject research protocols and bench studies.
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The Regulatory Coordinator is responsible for overseeing the day-to-day regulatory management of all types of clinical research protocols. Provide regulatory start-up support for research teams for all types of clinical trials.
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Writes and prepares Institutional Review Board (IRB) regulatory submissions, including, but not limited to, consent forms, new project applications, amendments, continuing review application, exceptions, and promptly reportable information.
$69,700 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The University of Alabama at Birmingham (UAB), Department Ped - Hematology/Oncology , is seeking a Clinical Research Regulatory Coordinator I. To assist with preparation of Institutional Review Board (IRB) submissions including preparing all relevant documentation and obtaining necessary signatures to meet study timelines.
$30.65 an hourFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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KEY RESPONSIBILITIES:Serve as the lead contact for assigned studies for collaborating physicians and staff, JAX Institutional Review Board, research staff and study participants.
$72,697.76Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Clinical Research Regulatory Coordinator will analyze and reconcile information from various sources to complete various regulatory based tasks, such as Institutional Review Board submissions and applications management, creation and maintenance of regulatory files, and quality assurance activities.
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Apply thorough knowledge of GCP (Good Clinical Practices), Institutional Review Board, and FDA (Federal Drug Administration) rules and regulations that apply to human subjects research.
$91,080 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Prepare regulatory documents for successful submissions to KPNWs Institutional Review Board. To execute and coordinate all clinical trial regulatory activities and requirements for the Clinical Research Support Services Department and to ensure compliance with all government regulations utilizing a formal quality management program.
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Generates reports and maintains files and documentation for compliance with regulatory requirements (federal and local agencies, including the Food and Drug Administration and Local Institutional Review Board) for the assigned study and/or clinical trial.
$46.42 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago
clinical research institutional review board jobs Title: coordinator regulatory
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