On-Site Study Coordinator

The On-Site Study Coordinator/Research Assistant role coordinates and supports remote site activities for clinical projects, serving as the primary point of contact for day-to-day communications and document submissions. Responsibilities include assisting with subject screening, re-consenting, data entry, and ensuring all activities comply with IRB and FDA policies under the direction of a Principal Investigator. Candidates will manage technology platforms, maintain accurate documentation, and assist with study closeout while adhering to ICH/GCP regulations.