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. Self-motivated and take initiative. Prioritize multiple projects and independently follow through with detail. Working Conditions This position has a hybrid work schedule which includes weekly in office
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recruiting and scheduling research subjects; assisting with developing or amending study protocols; assisting with developing data collection tools; assisting with building databases; and providing general
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scheduling research subjects; assisting with developing or amending study protocols; assisting with developing data collection tools; assisting with building databases; and providing general administrative
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assessments, data entry, and subject follow-up and scheduling. Research staff will be trained to administer quantitative sensory testing. Performs specific protocol procedures, such as specimens and data
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system operation and trouble-shooting procedures; coordinates with Associate Director, Operations to manage service, repair, and any additional technical training; develops and maintains schedule
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uploaded via the My Experience page, in the section titled Application Documents of the application. Job Family Research Role Impact Individual Contributor Scheduled Weekly Hours 40 Drug Test Required
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. Ensures that transaction verification procedures are followed with a limited degree of supervision. Responsibilities First point of contact when entering CRC. Assist with scheduling of visits on the CRC
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current policies and procedures, and federal regulatory requirements and guidelines. Sets schedule for each protocol under development and ensures that all members of the study team (study chair, committee
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soiled linen and distribute clean linen, prepare and transport instruments for sterilization, monitor level of clinic supplies, stock exam rooms and store new items upon delivery. Schedules patient
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/ Responsibilities include preparing and teaching seminar-style courses, holding regularly scheduled office hours, preparing and grading assignments, and attending staff meetings. The terms and conditions of