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We are seeking individuals with experience and research interest in: Clinical trials Patient outcomes Neuroimaging Neuro-technology Health services research and more Opportunities exist to collaborate world-class clinicians and leaders throughout the Neurological Institute which has almost 1,200 caregivers.
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Lead biomarker and pharmacokinetic planning, definition, and implementation, overseeing sample collection for early and late-phase clinical trials. Extensive oncology experience, including proficiency in target/disease biology, preclinical, and clinical development.
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This is an excellent opportunity to learn from some of the best in Oncology and be on the forefront of our new and emerging clinical trials and cancer research. Maintains professional growth and development through ongoing formal and informal education and clinical nursing study.
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Assist Clinical Scientist, Study Responsible Scientist (SRS), &/or Study Responsible Physician (SRP) in various clinical research assigned Immunology Development clinical trials.
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Knowledge and understanding of commonly-used concepts, practices, and procedures within the field of exercise physiology, epidemiology and those applied to clinical trials research. Working under general supervision, the research assistant will plan and carry out activities for a clinical research trial that involves exercise and psychotherapy in patients with comorbid pain and opioid addiction.
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Perform integrative analyses of multi-omics data from clinical trials and research cohorts, including genomics, transcriptomics, proteomics, and imaging, to identify biomarkers related to treatment mechanism and response, and potential therapeutic targets.
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If Associates Degree, must have minimum 6 years of work experience) Bonus points if: Experience designing Fund Accounting, Clinical Trials, Labor Costing, Effort Certification, and Pre-Award business processes within an Enterprise Resource Planning platform Experience working within hospital research/grants administration Proficiency in multiple business processes: (PTP, OTC, GL, FA, Budgeting, Cash Management, etc.
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Under the direction of the Manager - Sponsored Programs, maintains and monitors the administrative/financial aspects of grants, contracts, and clinical trials awarded to The MetroHealth System or Case Western Reserve University that will be conducted on the MetroHealth campus, and are funded by federal/state/private organizations/industry.
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Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.
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Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.
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Position Overview: As a Principal Statistical Programmer with a specialized focus on PK/PD, you will play a pivotal role in the design, execution, and analysis of clinical trials to support the development of our promising drug candidates.
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Leveraging your extensive knowledge of statistical programming and PK/PD principles, you will collaborate closely with cross-functional teams of scientists, clinical researchers, and biostatisticians to ensure the successful implementation of our clinical development programs.
$111,400 - $203,100 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Work Experience:New grad or less than one year RN work experience or if experience RN moving from non-inpatient to acute direct care clinical inpatient setting with less than one year current acute direct patient care RN experience.
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Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person. Enter source data into the sponsor's and/or vendor's data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator.
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The iBAM staff currently includes 100 members ranging from undergraduates to senior level Research Assistant Professors and supports research ranging from chemistry, to genetics, bioinformatics, and clinical trials.
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clinical trials jobs in Cleveland, OH
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