Responsibilities include coordinating day-to-day research activities; assisting with participant recruitment, screening, scheduling, informed consent, and study visits; collecting, entering, managing, and reviewing research data; maintaining study documentation and regulatory files; supporting IRB submissions, amendments, continuing reviews, and other regulatory requirements; assisting with biospecimen and/or neurobehavioral research procedures as applicable; conducting literature reviews and contributing to data analyses and development of reports, presentations, and manuscripts; and collaborating with investigators, clinicians, research staff, and external partners. Collaborates with Investigators and Research Managers in the preparation and execution of corrective and preventative action plans and ensures implementation and adherence to stated plan for low to moderately complex trials and non-therapeutic trials.