Clinical Research Nurse

About the role

The Clinical Research Nurse I works under the direction of the Principal Investigator to support complex research protocols involving investigational drugs, devices, or other interventions. The role serves as a liaison among the School of Medicine, clinical partners, IRB, and sponsors to ensure compliance with Good Clinical Practice throughout each study.

Key responsibilities

• Review and abstract medical record information, ensuring adherence to randomization, dosing, and administration schedules.
• Screen, enroll, randomize, and obtain consent from eligible patients.
• Schedule, perform, and supervise required study tests and nursing assessments.
• Document all study events and protocol procedures electronically and in writing.
• Verify clinical billing charges for accuracy and appropriateness.
• Enter study data into the clinical trial management system with accuracy and completeness.
• Maintain participant-level documentation, including access to EHR and charge routing.
• Identify and report adverse events, collaborating with the PI on attribution.
• Conduct visits for procedural and interventional studies and manage complex study orders in the EHR.

Required profile

• Knowledge of regulatory and institutional policies related to clinical research.
• Ability to work collaboratively with investigators, sponsors, and clinical teams.
• Strong attention to detail and excellent verbal and written communication skills.
• Capability to handle confidential patient data securely.

Required skills

• Proficiency with electronic medical records (EMR) systems.
• Experience using clinical trial management software.