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Under the direction of the Lead Lab Assistant, Laboratory Clinical Coordinator, Market Director of Laboratory Services and Laboratory Supervisor or Manager, the clinical laboratory assistant assists in specimen collection, receiving, processing, and distribution of specimens, clerical duties including accessioning, receptionist duties, processing specimens for Reference laboratory send outs, monitoring tube stations (when equipped) and distribution of samples.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Coordinate research program's logistics, including partnering with US and foreign sites for study supplies tracking and ordering, biospecimen transfer and cataloging, laboratory sample transfer and documentation.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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The Sample Coordinator will play a crucial role in our laboratory operations by accurately logging data into our Laboratory Information Management System (LIMS), managing sample inventory, and facilitating the smooth flow of samples for analysis by our chemists.
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Under limited supervision, this position in the Local Delivery Safety Translational Sciences (LDSTS) department is responsible for the technical support of in vivo studies in accordance with study protocols, Good Laboratory Practice (GLP) regulations, Standard Operating Procedures (SOPs), IACUC and departmental guidelines.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Must provide a personal DNA sample to be maintained by the Department’s Forensic Genetics Laboratory for quality assurance purposes. The Mission of the Harris County Institute of Forensic Sciences is to provide medical examiner and crime laboratory services of the highest quality in an unbiased manner with uncompromised integrity.
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Bowery Farming is seeking a Contract Laboratory Coordinator in our Kearny R&D Facility to build, maintain, and execute laboratory (Plant Pathology) methods, troubleshoot problems in the lab, and report results.
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Performs proficiency testing in compliance with Clinical Laboratory Improvement Amendments (CLIA) regulations i.e. analyze proficiency survey sample in the same manner as a patient specimens, no communication with other CLIA laboratories, complete record retention and accurate documentation and result reporting.
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Frontage’s core competencies include drug metabolism, pharmokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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Keywords : protocol, associate, oncology, cancer, clinical, clinical trials, clinical research, laboratory, protocols, data coordination, data coordinator, communications, research study, GCP, good clinical practices, translational science, medical research, protocol development, informatics, biospecimen bank merger, data harmonization, labtrack, sample tracking system, delinquency monitoring, tissue banks, SOPs, documentation, special projects.
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Provides support to Sample Coordinator and performs administrative tasks in the Sample Management department. Performs duties and training to acquire the skills required for sample and standard handling in support of the laboratory.
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Job Description:We are seeking a laboratory manager with excellent organizational and communication skills to help us catalog human samples received by the laboratory, interface with clinical partners to assure transfer of specimens, maintain the laboratory's regulatory compliance records, and manage day-to-day operations such as chemical waste management, purchasing, and supply management.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Laboratory Information System (LIS) upload the orders to activate label printing. Allscripts Pharmacy information, phone call back consent form, Task Bucket items, i.e. sample medications, written prescriptions, forms, etc.
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With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
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Collaborates with team members (Analytical Scientists, Quality Assurance, Material Coordinator, and Manufacturing Technicians) to meet timelines for drug product delivery. Performs routine and non-routine microbiology sample analysis (Bioburden, Endotoxin, Environmental Monitoring, Sterility, etc.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Reports to Director of Research Laboratory/Center Administrator and frequently communicate with Study Coordinator(s) with update on recruitment status. The Schiff Center for Liver Disease at the University of Miami has an exciting opportunity for a Full-Time Research Support Specialist to be responsible for the recruitment of study patients, including informed consents, sample collection, sample processing, shipping study specimens, creating and maintaining study logs, filing, assists with the preparing for monitor visits and FDA audits.
ExpandApply NowActive JobUpdated 6 days ago
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