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The Clinical Research Coordinator may coordinate device and drug treatment research trials, as well as observational studies conducted at Children's Medical Center, including but not limited to study set-up, implementation, fiscal monitoring, and data collection/entry.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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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 8 days ago - UpvoteDownvoteShare Job
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4 years of clinical research experience in the academic or pharmaceutical clinical trials environment. Relevant certification as a Certified Clinical Research Professionals (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professional (CIP) upon hire or within six months of hire.
ExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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As a Sr. CTA, you will work closely with the Clinical Operations team to support the full scope of study activities, including site activation, patient recruitment, study monitoring, and site and vendor management on Phase 3 trials.
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The Clinical Research Associate may be regionally based and is responsible for the monitoring of clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines and company SOPs, to support New Drug Applications.
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Purpose: The Clinical Research Services (CRS) team is made up of nearly 200 staff members who facilitate development, implementation, coordination, internal data monitoring, and completion of oncology-focused trials at Hillman.
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The Scientist will engage in innovative research in a dynamic team environment with a focus on developing and executing in vivo and in vitro evaluations to support target validation and drug discovery efforts for advancement into human clinical trials.
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Collaborates and supports Yale Center for Clinical Investigation (YCCI) Quality Assurance & Monitoring team on regulatory authority (e.g.: FDA, EMA) inspection preparedness for CTO supported trials as needed.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Responsible for the compilation of all data for clinical trials managed by the CTO. Manages project data including extraction, entering, processing, accuracy, analysis and evaluation of data ensuring that results meet project information and deliverable objectives.
$49,500 - $58,140 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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With the support of the study team, the research nurse will carry out state of the art clinical trials and other research studies, including consenting, screening, and enrolling eligible subjects, managing the treatment of patients throughout their participation in the study including education about any adverse effects they might experience, provide oversight and coordination of research testing and follow-up.
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Essential Duties and Responsibilities The major tasks for this position are as follows: Responsible for assisting with the planning and management of the operational aspects of clinical trials, including CRO and vendor management/oversight, ownership of various clinical trial tracking documents, ensuring project milestones and objectives are met and clinical study deliverables are consistent with program/company goals.
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Under general supervision is responsible for supporting the regulatory team with coordinating the research regulatory and administrative activities of clinical trials for the practice. Coordinates the preparation of regulatory submissions for new and continuing review of clinical trials.
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The Lead QC Microbiology Data Reviewer is an exempt level position with responsibilities for leading a team of microbiology data reviewers supporting the reviewing microbiology data and documentation generated from the Environmental Monitoring program, drug product and intermediates testing from the manufacturing facility utilized for cell therapy products for clinical trials and commercial operations in a controlled GMP environment.
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Implements proactive risk identification and mitigation planning for assigned clinical trial sites, leveraging Risk Based Quality Management (RBQM) principles and tools; executes activities relevant to all visit types (Site Selection, Site Initiation, Monitoring, and Closure) for assigned sites and clinical trials.
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Located just 30 minutes from the beach, TidalHealth offers the widest array of specialty and subspecialty services such as neurosurgery, cardiothoracic surgery, joint replacement, emergency/trauma care, comprehensive cancer care, wound care and clinical trials and research.
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clinical trials monitoring jobs
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