Sort by
Refine Your Search
-
/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
-
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
-
of reagents and supplies; optimize ordering and project scheduling to meet service expectations. Monitor instrument performance, oversee routine maintenance, and coordinate vendor support. Uphold SOPs, aseptic
-
health populations is preferred but not required. Work Schedule This position will be on site to begin and will be eligible for a hybrid work schedule combining remote and in-office work. The position is a
-
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