Research RN

Review studies for clinical and operational feasibility with the Investigator and Director of Research. Screen, consent, enroll, and follow study subjects while overseeing non-RN clinical research coordinators to ensure protocol compliance. Manage all data and source documentation, adverse experience reporting, and regulatory file maintenance. Prepare studies for IRB submission, ensure randomization and blinding procedures are followed, and verify eligible patient enrollment and consent processes. Enter quality data into sponsor databases, resolve queries, and prepare investigational products for administration. Ensure proper study drug accountability, storage, and dispensing. Assist with departmental policies and subject billing. Full-time Monday through Friday with no call or weekends. Willing to travel between offices.