RN Clinical Research Neurology

Prepare, evaluate, and implement research studies under principal investigator oversight, serving as primary coordinator for low to moderate complexity projects. Assess operational feasibility, develop budgets, prepare IRB documents, and institute protocol operations including data collection tools. Identify, screen, and enroll subjects per protocol while performing required research activities, assessing patient status, and documenting data into various systems. Maintain compliance with federal, state, and local laws, GCP, and institutional policies. Coordinate study activities such as adverse event identification, investigational product accountability, and specimen processing. Collaborate with study sponsors, CROs, investigators, and the multidisciplinary team. Requires Bachelor's degree in health or science, one year of clinical research experience, and Registered Nurse status with Michigan license upon hire. Basic Life Support (BLS) required within 90 days; ACLS, PALS, and specimen shipping training as needed. Full-time, 40 hours, 8:00 a.m. to 4:30 p.m. at Secchia Center, Grand Rapids.