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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 hourPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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.
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You will also support the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations.
$26.29 - $42.28 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Primary Responsibilities/Accountabilities: Screening and recruitment of potential patients for protocol eligibility. Serve as lead coordinator on a portfolio of Chemo/Onc research studies.
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CRCII is expected to conduct accurate data mining and extraction, work independently to meet deadlines and data base locks, interact, and communicate effectively with physicians, nurses and care managers among others to ensure the protocol is executed to the finest degree with minimal deviations or clarifications.
$55,120 - $99,340.8 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Working closely with regulatory partners 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.
$45,000 - $55,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Collaborate, develop and/or assist clinical leadership team on formulary management, protocol implementation, related education, medication use evaluations and integration of the electronic health records.
ExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Work with Study Coordinator to maintain screening and enrollment logs and track progress of patients on study while monitoring protocol compliance of specific study requirements. Preparation for study initiation and submission of required regulatory documents such as CV’s, Laboratory Certificates, FDA Forms, 1572’s, Financial Disclosure Forms, Training certificates, Delegation of Authority Forms, IRB submission and approvals, and other miscellaneous paperwork required for study compliance to study sponsor for each research protocol.
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