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Come join our team! The Clinical Research Budget Coordinator I develops clinical trial budgets for industry, National Institutes of Health (NIH), and investigator-initiated clinical research
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equipment is necessary for assignment to specialized areas, i.e. OR/ER, Sterile Manufacturing, ACP, Storeroom, etc. Schedule/Hours: Able to rotate shifts, alternate weekends, and rotate throughout any areas
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clinical research staff in day to day operations. Provides input in the performance review of the staff. Coordinates and leads routine research meetings. Works on both industry sponsor initiated and
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The Associate Director, Strategy is responsible for evaluating, analyzing, and making recommendations on new business development opportunities and strategic plans. The role is responsible
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decontamination and clean assembly areas in a safe and technical manner consistent with department and CSHS policies and procedures. Inspects and assembles instrument trays, using content lists and Manufactures
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decontamination and clean assembly areas in a safe and technical manner consistent with department and CSHS policies and procedures. Inspects and assembles instrument trays, using content lists and Manufactures
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, translational, regulatory and manufacturing, Cedars-Sinai is committed to pushing the frontiers of medicine and discovering new technologies and innovations that will impact how we diagnose and treat disease
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responsibilities: Assists in establishing processes and procedures for all Quality Assurance (QA) and Quality Control (QC) functions of the SOCCI Clinical Research Office (CRO) to include industry sponsored studies
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(QC) functions of the SOCCI Clinical Research Office (CRO) to include industry sponsored studies, investigator-initiated studies, and cancer cooperative group trials Conducts routine and for-cause
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clinical incidents involving medical devices and disseminating information to all necessary parties. Communicates to manufacturers about problems with medical devices and ensures appropriate response