Clinical Research Nurse – Internal Medicine

About the role

The Clinical Research Nurse I supports complex internal‑medicine research protocols, acting as a liaison among the School of Medicine, clinical partners, investigators, IRB and sponsors. The role ensures adherence to Good Clinical Practice throughout each study’s lifecycle.

Key responsibilities

• Review and abstract medical records, enforce randomization and study‑drug dosing.
• Screen, enroll, obtain consent, and schedule participants according to protocol criteria.
• Perform or supervise study‑specific tests and nursing assessments.
• Document all study events in paper or electronic formats and enter data into the clinical trial management system.
• Verify clinical billing charges for accuracy and appropriate routing.
• Apply regulatory and institutional policies to study documentation, submissions and SOPs.
• Identify and report adverse events, collaborating with the Principal Investigator on attribution.
• Maintain participant‑level documentation, including access to EHR and charge routing for complex studies.

Required profile

• Strong knowledge of regulatory and institutional research policies.
• Proficiency with electronic medical records and related computer applications.
• Excellent verbal and written communication with high attention to detail.
• Ability to work with web‑based research platforms and data‑entry tools.

Required skills

• Electronic Medical Records (EMR) systems
• Clinical Trial Management System (CTMS) usage
• Web‑based research applications

What we offer

• Opportunity to work on cutting‑edge investigational drug and device studies.
• Collaboration with a leading academic medical center and health‑care partners.
• Professional development in clinical research and regulatory compliance.