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, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. Responsible for accurate and timely data collection, documentation, entry and reporting, including
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of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and
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timely data collection, documentation, entry and reporting, including timely response to sponsor queries. Schedules and participates in monitoring and auditing activities to ensure compliance, including
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related records Transports, processes and logs samples Maintains computer database with relevant clinical information. Performs lab maintenance duties, including glassware cleaning and sterilization
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the study. This role evaluates and abstracts research data and ensures compliance with protocol and research objectives. Position is responsible for completing case report forms, entering clinical research
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procedures throughout training period. May develop, adapt, and implement new research techniques and protocols. Analyzes and interprets data. May assist in preparation of grant proposals. Participates in
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supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. Supports objectives of research studies through noncomplex tasks such as data collection
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in tasks supporting the coordination/implementation of noncomplex research studies. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential
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may develop, adapt, and implement new research techniques and protocols. The team member analyzes and interprets data, may assist in preparation of grant proposals, and participates in publications and
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of research studies through noncomplex tasks such as data collection, prescreening of and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring