Clinical Research Nurse 2 - Full-Time, Miami FL

Requirements

• as specified by MSOM, UHT, JHS, and other relevant entities (including Citi Training, Bio Safety, Lab Safety, OSHA, and HIPAA). Participate in quality review to ensure accurate and compliant documentation. Reviews Serious Adverse Events documented and reported per the protocol and regulatory requirements for protocols serviced by the CTRS. Work closely with principal investigators and staff across multidisciplinary teams to ensure seamless protocol execution and high-quality patient care. Demonstrate knowledge and understanding of policies, procedures, and regulations governing human subject research. Implementation of clinical trial protocols requiring CTRS services, ensuring adherence to Good Clinical Practice (GCP), FDA, HIPAA, and IRB regulations. Assess and document protocol-related patient compliance and response to treatment according to physician treatment orders. Educate staff about protocols related to treatment, possible side effects, and complications. Enter research-related orders and results in UChart / Cerner as per protocol. Receive Investigational Products from Research Pharmacy and administer the drug according to physician treatment orders. Serve as primary contact for PIs, staff, and departments regarding protocol-related issues to ensure a safe environment for patients while maintaining compliance and adhering to regulatory guidelines. Assist in participant recruitment, screening, informed consent process, and retention efforts when required. Maintain a safe working environment by adhering to established policies and procedures within the unit. Ensure alignment with the University's strategic mission, vision, values, and Code of Business Conduct in planning research-related patient care and clinical research.

How this role fits you