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Under minimal supervision is responsible for the research regulatory and administrative activities of clinical trials for the practice. Ensures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations through OSHA, CDC and HIPPA. Supports and adheres to US Oncology Compliance Program, to include the Code of Ethics Business Standards.
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Study Team Leader and primary operational contact for 1-3 trials of average design and protocol complexity, including clinical trials, Rx-to-OTC Switch & associated behavioral studies, and decentralized/virtual trials.
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This is a full-time on-site role for an Assistant Clinical Research Coordinator at Oregon Dermatology and Research Center located in Portland, OR. The Assistant Clinical Research Coordinator will be responsible for day-to-day tasks related to clinical research, including administrative and clinical support, lab processing and shipping, protocol implementation, recruitment and retention, and data collection.
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Supports and monitors clinical trials to ensure sponsor and investigator obligations are met and in compliance with the currently approved protocol/amendment(s); applicable study procedures; applicable federal and local regulatory requirements; GCP; and company policy and procedures.
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The Rater is responsible for the organization, administration, management, and efficient execution of clinical ratings associated with clinical trials. Manage aspects of the study related to ratings with the rater training representative, study sponsor, Site Director, and Principal Investigator to ensure compliance with protocol requirements.
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We are currently seeking a Board Certified Dermatologist to assist our Medical Director and staff, in the review of clinical trial protocols, and participate in those trials, by providing your services in performing general dermatology examinations, in accordance with the authorized protocol.
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Onsite) FUNCTION: Clinical Operations – Biomarker and Bioanalytical Operations Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Company therapeutic areas.
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The budget specialist is responsible for reviewing the Medicare coverage analysis, protocol, sponsor proposed budget and informed consent (if available) and fully accounting for all clinical costs and investigator and study team effort required to carry out the study, as well as costs for ancillary services.
$81,873.83 - $95,000.04 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Senior Clinical Trials Manager is responsible for oversight and execution of the operational aspects of one or more clinical studies from protocol development through database lock.
$150,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Manages and coordinates all facets of assigned clinical protocols from IRB preparation through query and data seal; ensuring protocol and regulatory compliance. The Ivy Brain Tumor Center is a non-conventional, non-profit program offering state-of-the-art clinical trials for patients with the most aggressive form of brain cancer.
$30.55 - $44.3 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - 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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4 years of clinical research experience in the academic or pharmaceutical clinical trials environment. Trains and mentor, entry level Clinical Research Coordinators, Regulatory Coordinators, Research Protocol Coordinators, students, residents, and fellows on the basics of regulations applicable to clinical research.
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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.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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The range of these research projects are extensive and comprehensive, extending from biomarker/natural history studies to Investigator Initiated studies to Industry clinical trials (Phases 1-3.
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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 2 days ago
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