Clinical Research Coordinator, RN

Clinical Research Coordinator, RN's are primarily responsible for study coordination and data management, with a central focus on managing subject recruitment and enrollment, consistency of study implementation, data management and integrity, and compliance with regulatory requirements and reporting. Responsibilities include maintaining site compliance for clinical trial activities, maintaining knowledge of FDA regulations, ICH-GCP guidelines, SOPs, completing required training, educating and directing protocol compliance, managing protocols with clinical complexities, ensuring good documentation practices, communicating with stakeholders, acting as patient advocate, collaborating with scheduling staff and physicians, and adhering to ethical conduct and HIPAA compliance.