About the Role

This position is responsible for coordinating the operational, administrative and regulatory activities associated with human subjects research studies and research programs. The role supports investigators and research teams with study start up, regulatory submissions, essential document management, research tracking, scheduling, and general study administration to ensure compliant and efficient research operations. This position works collaboratively with investigators, research nurse coordinators, sponsors, CROs, and institutional stakeholders to support study activation, regulatory compliance, audit readiness, and ongoing research administration. This is a non-clinical position and does not involve direct patient care, clinical procedures, informed consent, or participant-facing research activities. The role is intended to support operational efficiency within the research program by coordinating non-clinical research activities.

Responsibili...