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, communication, organizational and problem-solving skills the ability to work under tight schedule to meet project deadlines the capability to work both independently and as part of a team experience with advanced
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limited to the following: Screen, recruit, provide informed consent, and enroll participants according to protocol for clinical studies. Schedule participant study visits in coordination with laboratory and
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/or Clinical Trials Protocols. Support the preparation for IRB audit and monitor: Assist in the preparation of IRB applications, amendments and scheduled continuing reviews, progress reports, safety
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and/or qualitative data collection Work Schedule Our team members have the option to work four 10-hour shifts or five 8-hour shifts per week. Shift times are usually between the hours of 10:00am - 8
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setting. Ability to effectively communicate with staff and faculty of all levels. Knowledge of university policies and procedures is desirable. Work Schedule Hours/Week: 40 hours Shift as assigned