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of the Center Director and Associate Director, this person will be independently manage, coordinate, and provide oversight of clinical research study conduct across multiple research studies and trials
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to biomedical research • Strong organizational and time management skills; ability to manage multiple tasks simultaneously and meet established deadlines. • Familiarity with basic computational tools such as
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performed • Ability to perform, manage, and balance multiple projects and tasks simultaneously, work under time constraints, and meet deadlines • Proficient in various software programs (including database
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, Statistics, or a related field. • Experience working with relational databases with multiple tables. • Experience with database management, analysis, and database visualization and reporting tools
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to interact diplomatically, professionally, and courteously with internal and external colleagues. • Excellent organizational skills; ability to prioritize work assignments and manage multiple projects
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contracts management • Proficient use of computers; requires solid working knowledge of MS Office Suite (Word, Excel, PowerPoint) • Ability to manage and prioritize multiple projects/tasks simultaneously
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presentation software. Ability to manage multiple tasks and projects simultaneously Ability to prioritize work, performing assignments with minimal supervision Required Education and/or Experience Terminal
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Word, Excel, Outlook, etc. • Expert in time management and flexibility with multiple demands. • Ability to establish work assignment priorities and perform duties independently, without immediate
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skills, attention to detail, and the ability to plan ahead • Excellent time management skills and the ability to meet established deadlines • Ability to work independently, manage multiple priorities, and
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members. The RegulatorySpecialist provides operational support for regulatory compliance and is ableto independently provide regulatory support to the TCC PI and research sitesconducting multiple FDA