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Oversee the full life cycle of multicenter randomized clinical trials including study design and implementation; data collection tool development; data quality assessment and ongoing monitoring; regulatory reporting; statistical analysis; interpretation of results and manuscript writing for the Peripheral Artery Disease (PAD) research group.
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The Clinical Research Coordinator (CRC) will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical studies, ensures the timely collection and management of protocol-related samples, maintains regulatory binders, and ensures study compliance with state, federal, and IRB requirements.
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Our mission is to provide the best clinical care to our patients, investigate the most promising advances in neuroscience research, and train tomorrow's leaders in neurosurgery. Performing and documenting clinical IHC work: test slides, controls, instrument logs and pathologist review sheets as required by CLIA standards.
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Reporting to the Breast CRG Clinical Research Manger, the Clinical Research Coordinator Associate - Breast Oncology will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to ensure protocol requirements are carried out and data quality is maintained.
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In this role, the Clinical Data Manager (CDM) will be responsible for performing core data management functions for Phase 1, Penn-Sponsored clinical research studies as follows:Data Quality/IntegrityPerform study level database training (End User and Sponsor Teams); Create/manage study database training curriculum; Perform re-education/training as needed.
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Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.
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Ensure Network patients follow through with referrals to other specialties, labs, and diagnostic imaging through review of patient records in OHSU Epic and through direct verbal and written communication with representatives from Network Member clinical teams and OHSU clinical and research teams.
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As part of the Pearson Clinical Psychometrics team, psychometricians are responsible for providing psychometric services (consulting, data analysis, psychometric review) for the research and development of Pearson clinical assessment instruments.
$85,000 - $90,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Serve as lead psychometrician on the assigned research projects from Pearson Clinical Assessment. Review and approve all research specs and ensure the most appropriate psychometric procedures and research design are used for the assigned research projects.
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This role will also work closely with global and regional (Osaka, Japan [SHQ]; Florham Park, New Jersey [SI]; and London, England [SEU/SBV]) cross-functional team members including Medical Affairs, HEOR, Clinical Development, Regulatory, Market Access, Commercial teams and external collaborators/vendors to lead and conceptualize research questions, propose study designs, identify appropriate databases, write and review protocols, oversee data analyses, reports, presentations, and publications.
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In this role, you will have the opportunity to:Manage a team of Clinical Research Associates assigned to site management and data review of a new cardiac enrollment study, which involves active mentoring, regular coaching, and developing people to build skills and elevate capabilities.
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Collect and manage patient and laboratory data for clinical research projects. We seek a Clinical Research Coordinator Associate – Breast Oncology to help us enact our mission to reduce cancer mortality through comprehensive programs of cancer research, treatment, education and outreach.
$31.73 - $36.54 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Design, implementation and project management of in vivo syngeneic tumor model studies with various CROs. This will include coordinating experimental design meetings between the INTO team and CRO, review and finalization of workorders, monitoring of ongoing studies and data analysis and presentation of results Drug Discovery Project Leadership: Leadership of pre-clinical drug discovery projects of the INTO immune-oncology portfolio.
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The Clinical Data Coordinator (CDC) will collect, abstract, review, document and monitor data related to clinical research projects. The CDC is responsible for working collaboratively with the Research Nurse Clinician, Clinical Research Coordinator and Clinical Lab Coordinator in the coordination and collection of data for cancer clinical trials.
$26.13 - $39.2 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Assists in preparing grant applications and documents (e.g., Institutional Review Board, Grants, and Contracts Office), and provides clerical support to Clinical Research Coordinators and others in assigned areas.
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