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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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We are seeking a leader with broad non-clinical development experience, including preclinical and IND-enabling protocol development and execution, pharmacology, toxicology, DMPK, and bioanalysis.
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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 Today - UpvoteDownvoteShare Job
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Machine Learning Model Development: Design, develop, and implement machine learning and deep learning models to address specific challenges in clinical trials, such as patient recruitment, data analysis, protocol study, anomaly detection, document entity extraction, document generation, translation, and outcome prediction.
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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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Using a disease-specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB processing, patient recruitment, study coordination, study-specific training, data collection, and specimen collection and processing.
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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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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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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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The position will work closely with the members of the clinical research team to develop effective tools for close monitor and reporting of trials accrual and coordinate the timely study activation and submission of protocol amendments.
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The clinical trials involved encompass various drug therapeutics, including chemotherapy, immunotherapy, targeted therapy, and cell therapy. The ideal candidate will be a Senior Research Nurse with current or previous leadership experience and direct involvement in managing drug therapeutic clinical trials.
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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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The Clinical Research Coordinator II is able to recruit, follow, and retain study participants, and perform study visits, data collection and entry, and quality control activities according to study protocol independently.
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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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Working closely with our data & analytics team and clinical trial experts, this role will harness the power of cutting-edge AI and LLM (Machine Learning and Deep Learning) technologies for enhancing decision-making in the field of clinical trial process.
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clinical trials protocol jobs
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