Registered Nurse (RN) - Research - Full Time, Days

Role Overview Responsible for implementing, managing, and overseeing research studies, including educating research staff, healthcare team members, participants, and caregivers. Manages clinical data, monitors study compliance, and ensures efficient data flow for patients in clinical trials. Coordinates patient visits, implements protocol procedures, and tracks participant progress and safety issues, communicating with investigators and regulatory agencies. Key Responsibilities Assist in determining patient eligibility and facilitate participation, including informed consent.Evaluate outcomes, communicate with the healthcare team, and adjust patient care based on protocol requirements.Collaborate with interdisciplinary teams to develop care plans and educate staff on trial procedures.Provide patient and family education regarding clinical trials, treatment, potential side effects, and self-care.Collect, document, and review study data to ensure regulatory compliance, preparing for audits and study visits.Manage study inventory, supplies, and medication, and coordinate with sponsoring agencies and IRB.Supervise research staff, ensuring practice within qualifications, training, and optimal team functioning.Support resource coordination, develop data collection tools, and contribute to research program growth.Maintain professional development through seminars and literature, and participate in educational presentations. Qualifications & Skills Associate degree in Nursing required; Bachelor's preferred.At least one year of nursing experience, research experience preferred.Current RN license recognized in the practicing state. Additional Details This role reports to a supervisor but does not have management responsibilities. It involves day shift work at a hospital facility, supporting upstate research operations.