Registered Nurse - Clinical Research Coordinator III

Benefits

Qualifications

• •ASN or BSN required
• •Active Registered Nurse (RN) license required
• •Minimum 2–5 years of nursing experience required
• •Strong understanding of clinical research protocols and regulatory compliance
• •Valid Driver’s License required
• •Qualified candidates interested in this opportunity are encouraged to apply or contact us directly for more information
• •3 more items(s)

Responsibilities

• •Schedule: Monday to Friday, 8:00 AM – 5:00 PM
• •The Clinical Research Coordinator III (RN) is responsible for coordinating and managing clinical research studies under the supervision of the Principal Investigator
• •The role involves handling Phase I–III interventional clinical trials, ensuring compliance with GCP, ICH/FDA guidelines, regulatory standards, protocol implementation, patient safety, data integrity, and research operations
• •Coordinate patient care for clinical trial participants
• •Review study protocols and ensure protocol compliance
• •Perform subject eligibility assessments and informed consent procedures
• •Monitor adverse events and ensure timely reporting
• •Maintain investigational product accountability and research documentation
• •Manage IRB/IEC documentation and regulatory submissions
• •Ensure accuracy and integrity of clinical trial data
• •Support monitoring visits, audits, and CAPA processes
• •Assist with clinical trial budgeting and research billing compliance
• •9 more items(s)