Clinical Research Coordinator III

Assist with daily human subjects experiments (lab or participant homes) - health monitoring, questionnaires, equipment setup for neural recording/stimulation, video monitoring, execution of experiments, Document experiments in daily test log, Run core clinical trial experiments independently; basic hardware/software troubleshooting, Provide skin care for percutaneous neuroprosthetic devices; train caregivers on skin care around devices, Supervise visitors/collaborators observing or participating in experiments, Professional interaction with research participants; Ensure personnel/equipment readiness for daily experiments; Ensure experiments conducted per University, IRB, and FDA regulations.

Track milestones/deliverables for ongoing projects, facilitate meetings and information sharing, identify risks to study completion, Coordinate reporting; serve as primary point of contact for collaborators, Assist PIs/Operations Manager with visitor coordination, materials transfer agreements, data sharing agreements.

Lab and physical space management (preparing, maintaining, organizing), Develop software/hardware to facilitate experiments or documentation, test all equipment/paradigms prior to participant arrival, navigate code/configuration versions using Git, Coordinate study staff/trainee coverage; maintain lab wiki and written protocols, Communicate with participants/families regarding scheduling, Schedule equipment service calls

Data management: transfer data to lab server, summarize for scientific/regulatory reports, Lead efforts to fulfill data sharing requirements (funding/publication), Train new team members; evaluate readiness to lead experiments, run data analysis scripts to generate figures, liaise between participants, trainees, and regulatory/fiscal staff, provide information for scientific/regulatory reporting, Assist with participant payments/reimbursements