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Description Clinical Research Coordinator B ResponsibilitiesThis individual will work under general supervisionThe CRC will be responsible for the coordination of complex oncology clinical research protocols, including accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing study protocol training.
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Clinical Research Coordinator work includes study design, protocol development, submission to review boards, subject recruitment and enrollment, study visits and regulatory compliance in one or more studies.
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Schedule: Monday through Friday 8 AM to 4:30 PM Job Summary: The Clinical Research Coordinator collects, prepares and distributes information necessary for protocol development and study initiation at the Rothman Institute Orthopaedics.
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In addition to the responsibilities above, the Clinical Research Coordinator C will coordinate supply management, track experimental drug and device use (accountability), and find creative solutions for various logistical problems to protocol implementation.
$77,315 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Protocol Coordination - Follow study protocol procedures, providing input as appropriate for changes, updates and revisions to survey instruments and data collection procedures. Identify and report needed protocol and procedural changes, coordinating the ongoing implementation of the research protocol, and defining recruitment and retention strategies.
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Demonstrate a comprehensive clinical knowledge of treatment indications, assist with organizing weekly conferences, protocol follow up, education, and clinical care of patient. Work collaboratively with physicians to provide community education, first responder education, as well as peer education within Cooper University Health Care.
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The day-to-day assignments for executing clinical trials will include study activation, process design and execution of study procedures as outlined by the study protocol (and related documents), screening potential participants, chart abstraction, survey administration, data reporting to sponsors and facilitation of monitoring visits and audits.
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Runs portions of clinical trials from startup to closeout, including protocol coordination (screening, recruiting, enrolling, consenting), feasibility planning, data management, biological specimen management, preparation for monitoring visits, and regulatory and/or IRB document preparation.
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Prepares and submits all materials for the Institutional Review Board (IRB) and other regulatory bodies as required by the protocol to ensure compliance in a timely fashion. Ensuring all study procedures are conducted according to the protocol and applicable regulations.
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The Clinical Research Coordinator collects, prepares and distributes information necessary for protocol development and study initiation at the Rothman Institute Orthopaedics. He or she maintains integrity & quality of research data, patient enrollment process, data analysis for various medical publications & reports, protocol implementing, research data base management, & IRB submission.
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Maintains appropriate receipts and financial records as per EHC dispensary protocol. Accurately collects all prescription co-pays or payments from patients prior to dispensing medicines as per EHC dispensary protocol.
$19.23 - $24.99 an hourFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Review all assessments with the AOC and requests labs per Gift of Life and hospital protocol. The Referral Coordinator will ensure timely on-site response, assessment, and evaluation of potential organ donors , as well as interacting with the hospital staff to set-up the family approach process.
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Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials. DM Clinical Research, the largest privately-owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for an Unblinded Clinical Research Coordinator to join our team.
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