The Study Coordinator will be involved in studies examining the effects of interpersonal trauma and/or brain injury on mental, cognitive, and neurological health. They will be responsible for completing participant recruitment, scheduling MRIs, performing informed consent and participant assessments, as well as study organization including data collection and curation. They will also assist with the preparation and submission of grant applications and regulatory documents (e.g., Institutional Review Board, Grants and Contracts Office). This work will be under the supervision of the Principal Investigators (Drs. Elisabeth Wilde and David Tate) and senior clinical research staff.