130 security-"https:" "https:" "https:" "https:" "UCL" uni jobs at Cedars Sinai Medical Center
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regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines. Assists with
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submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines. Responsible for sample preparation and shipping and maintenance of study supplies and
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systems to ensure protocol compliance and patient safety. Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion
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to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines. Assists with clinical trial budgets and patient
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perform a variety of routine experimental protocols and procedures to support the objectives of laboratory research projects. The incumbent will observe and follow safety standards and procedures, assist in
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-project-oriented labs. Organize clinical and research trials in conjunction with the Principal Investigator and sponsor and funding source. Monitor and ensure compliance with safety standards and procedures
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Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines. May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with
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to submit Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines. Assists with clinical trial budgets and patient research billing as needed Schedules
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detailed data collection, and analysis, operation and maintenance of specialized equipment. Excellent written and oral communication skills are essential. Knowledge of safety standards. Req ID 9179 Working
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coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines May