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Clinical research, Oncology, inpatient, Gcp, Irb, Data management, BLS, CPR, AED, Registered Nurse, communication and leadership skills, CCRC or CCRP Certified, patient registration, quality assurance, subject eligibility, EMR, clinical trial, regulatory, oncology nursing, chart review, enrollment, adverse event reporting.
$30 - $45 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Reporting to the Regulatory Affairs Manager, the Regulatory Affairs Specialist will, with minimal supervision, prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all applicable regulatory review committees- including new submissions, continuing reviews, amendments, adverse events, and reportable events.
RemoteExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Understanding of IRB, and/or IACUC (Institutional Animal Care and Use Committee) research protocols and process. Coordinate administrative, IRB, and/or IACUC (Institutional Animal Care and Use Committee) approval of proposed research protocols.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Work with P.I.s to submit applications for IACUC or IRB approval, quarterly effort confirmation, and re-budgeting requests. UT Southwestern Medical Center is hiring for Senior Grants and Contracts Specialist, Biomedical Engineering.
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Will work closely with the clinical researcher to assist with project development, cohort definition, data collection, tool development, IRB proposal, Sentara Portal submissions, and other project tasks as assigned.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Coordination with the relevant parties of any Material Transfer Agreements, IRB and or IACUC and or PBIC protocol approvals/amendments as needed. As part of the Grants Management Team under the direction of the Sr. Admin Manager, the Grant Administrator will assist the departmental level grant and contract administration (Sponsors include (not limited to): DOD, NSF, NASA, NIH, of a midsize portfolio of foundation awards, contracts, and billing agreements.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Institutional Review Board (IRB) preparation; developing data collection instruments; assisting with building databases; subject recruitment, screening, data collection and centralized data entry.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Manages, maintains, and ensures laboratory compliance to the human subjects (IRB), biosafety (IBC), and animal usage (IACUC) protocols. Manages, maintains, and ensures laboratory compliance to the human subjects (IRB), biosafety (IBC), and animal usage (IACUC) protocols.
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Complete all training required by BMC IRB, central IRBs, NIH, and NIDA Clinical Trials Network. Liaisons with Institutional Review Board (IRB) for submissions, correspondence, and regulatory binders, including administrative amendments.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Assist with preparation and processing of all Institutional Review Board (IRB) documentation including submissions, continuing reviews, amendments and adverse event reporting. Work with the regulatory manager to ensure that submissions to the IRB are completed in a timely manner.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Division of Cardiology at Pennsylvania Hospital seeks a full-time Clinical Research Coordinator to organize, coordinate and implement complex studies involving a wide variety of investigational products/devices and various sponsors.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Review "informed consent" with patient; coordinate and educate patient and medical personnel as to required follow-up tests to be performed; assist physician in preparing IRB documents and maintain correspondence with sponsoring company/agency and IRB. Assure adherence to study requirements according to protocol; monitor study drug according to protocol; monitor and/or perform pharmokinetic studies as detailed in protocol and attend to laboratory procedures to process, store and ship specimens.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Responsibilities Will be responsible for assuring compliance with study protocols, including IACUC and IRB, and laboratory safety. Will perform routine cellular and molecular assays (e.g., transformation, miniprep, maxiprep, RNA, DNA and protein preparation, cDNA synthesis, qRT-PCR, transfection, packaging of viral vectors, ELISA, Western Blotting, etc.
$51,839 a yearExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Prepare institutional review board (IRB) protocols, material transfer agreements (MTAs), data sharing agreements (DSAs), shipping and receiving of samples from ongoing studies. Proven experience in the following scientific techniques and procedures is preferred but not essential: Human tissue processing, immune cell isolation, transfections, flow cytometry analysis, and immunohistochemistry.
ExpandApply NowActive JobUpdated 8 days ago
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