Research Associate I

Conduct screening and pre-screening activities to identify eligible study participants.Review medical charts and extract relevant data for research purposes.Prepare and submit Institutional Review Board (IRB) applications and amendments and manage different types of IRB submissions.Effectively communicate with Principal Investigators (PIs) and other clinicians to ensure smooth study pleting transcranial magnetic stimulation training and delivering TMS to trial participants.Work both independently and as part of a team to achieve project goals.Maintain detailed and accurate records of all research activities, including regulatory submissions and correspondence.Ensure research program and projects are in full regulatory compliance.

Created: 2025-10-06