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Clinical Research Coordinator C (CRC-C): In addition to above, the CRC-C will have limited supervision from the project manager and will need to use more independent judgment when managing their assigned clinical trials.
$42,953 - $77,315 a yearExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Our Plano campus is looking for an experienced Clinical Research Coordinator who will play an important part in coordinating drug treatment research trials within the Hematology and Oncology teams, as well as observational studies.
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The Clinical Research Coordinator assists the clinical trials process by registering hematology, oncology, and bone marrow transplant patients for clinical studies, assessing eligibility criteria, maintaining current protocol packets and assuring that all quality assurance measures are maintained within the protocol/study.
$39,300 - $64,349 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Experience 2-5 Years' experience as a Clinical Research Associate, Clinical Research Coordinator, Clinical Research Nurse Coordinator and proven experience as an Lead Auditor.
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The Clinical Research Nurse Manager supervises compliance and educational activities within the Institution as it relates to clinical trials and preclinical studies. Research certification is required, including CCRP (Certified Clinical Research Professional) or CCRC (Certified Clinical Research Coordinator), or OCN certification; with research certification obtained within 6 months of hire.
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Responsible for coordinating clinical research activities for the FPBCC. Assist UNMC Principal Investigators and nurse coordinators with project management, coordination and implementation of clinical trials.
$51,200 - $76,800 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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The Knight Cardiovascular Institute Senior Clinical Research Coordinator is responsible for various duties related to clinical trials. The Senior clinical research coordinator is also the primary liaison for patients receiving care on a clinical trial and is responsible for the triage of patient needs.
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As a Junior Clinical Research Coordinator, you are responsible for assisting with the management and coordination of all aspects of conducting clinical trials within s RII, surgery centers, both clinically and administrative/regulatory.
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Join other professionals revolutionizing efficient and seamless study start-up to advance clinical trials. We have openings for clinical research coordinators to best match your experience level.
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This position will manage activities pertaining to the Protocol Review and Monitoring Committee (PRMC) which primary goal is to ensure that institutional, industry-sponsors, and externally peer reviewed cancer research studies involving human subject conducted under the auspices of the SCCC are (1) scientifically and statistically sound; (2) appropriately designed; (3) feasible for completion; and (4) if applicable, in compliance with NIH guidelines for clinical trials.
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This unique role allows for the clinical research nursing professional to work in the community and screen/enroll patients in all cancer disease centers with UPMC Hillman Cancer Center working as a Trials Coordinator.
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This is a clinical research coordinator position within the Hematology department. The Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator.
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As a member of The US Oncology Network , one of the nation's largest community-based cancer treatment and research networks, Compass Oncology participates in leading-edge clinical trials through US Oncology research, which has helped develop 89 FDA approved cancer therapies.
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Keywords: Clinical Research Coordinator, Cardiac Research, Monster, Clinical Research Associate, Talroo-Allied Health. Sentara Norfolk General Hospital located in Norfolk, Virginia is seeking a Clinical Research Coordinator for the Cardiac Research Department.
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The Clinical Research Coordinator (CRC) is central to conducting and managing clinical trials, tasked with obtaining informed consent, executing study protocols, handling human specimens, and ensuring meticulous documentation and communication.
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