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the correct provision of technical services for events. Monitor and track equipment usage for each event to ensure accurate event billing. Maintains effective communication with auditorium staff,university
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clinical research studies. Oversee investigational product (IP) receipt, storage, accountability, tracking, and dispensing activities. Prepare studies for monitoring visits, audits, site visits, and closeout
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systems and asset tracking. Demonstrated success leading technology-related projects and cross-functional initiatives. Experience developing and maintaining spreadsheets, analyzing data, and preparing
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, including ordering and inventory of reagents and supplies; organization and tracking of cell lines, organoid models, cryopreserved stocks, samples, and associated records; freezer and storage organization
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regulatory and study documentation, including regulatory binders, delegation logs, enrollment tracking, adverse event reporting, and compliance with institutional and federal requirements Administer clinical
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, storage, tracking, accountability, and participant dispensing. Serve as a primary liaison among sponsors, investigators, regulatory offices, research support services, and study teams. Prepare and maintain
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system and its reports to manage research participants' activities, calendars, tracking/marking financial milestones, and all aspects of study visits. Uses required EMR functionalities to manage
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execution. Track and manage progress to achieve project milestones, deliverables, and timeline goals through collaboration with colleagues, subcontractors/vendors, and external stakeholders. Coordinate
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concise materials for stakeholder and expert review and response. Track and manage progress to achieve project milestones, deliverables, and timeline goals through collaboration with colleagues
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leadership across multiple study teams in sponsor and CRO communications, site visit management, protocol and participant tracking systems, study feasibility assessments, resource allocation, and financial