ResponsibilitiesManage and coordinate research and administrative needs for scientists.Navigate regulatory procedures and assist with study design.Develop and execute research protocols.Procure lab equipment and supplies.Monitor project timelines and reportingManage single and multi-site clinical trials including study start-up, daily operations, troubleshooting, QA & QC, SOP development, and study close-out activities.Interface with PIs, clinicians, researchers, staff, and collaborators.Supervise clinical research coordinators, student workers, and research assistants.Educate and train all lab personnel to administer TMS and TES.Essential SkillsStrong experience in human subjects research.Experience in cognitive neuroscience is required.3-5 years of experience in clinical research, protocol development, regulatory processes, IRB, and GCP.Experience in clinical trials, protocol design, regulatory processes, data review, and timeline management.Work Environment
The role requires working 5 days on campus across 2 locations
Occasional work from home is possible in certain situations. The team consists of 6 clinical research coordinators and 4 principal investigators.
Pay
The role will pay $70k-$74k/yr based on relevant experience
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