RN Protocol Coordinator - Clinical Research

University of Southern California; Glendale (CA); On-site; USD 68,880 - 86,788; Full time

Job summary

The University of Southern California (USC) seeks an experienced Registered Nurse to join the clinical research team as Protocol Coordinator. The role requires independent work, collaboration with physicians, patients, data managers, and hospital staff, and adherence to hospital policies.

Responsibilities include protocol review, patient eligibility, informed consent, data entry, SAE reporting, and training other coordinators.

Qualifications

• Bachelor's Degree required.
• Current California Registered Nurse license.
• Minimum one year experience in clinical research or related field.
• Ability to work independently and adhere to SOPs.
• Completes required HIPAA, GCP, and safety trainings.

Responsibilities

• Review protocols for feasibility and dosing considerations.
• Ensure study conduct aligns with protocol and regulatory requirements.
• Enter patient data and manage SAE reporting per FDA guidelines.
• Coordinate patient eligibility and informed consent processes.

Skills

Independent worker

Clinical research

Team collaboration

Communication skills

Education

Bachelor's Degree

Job description

The University of Southern California (USC) seeks an experienced Registered Nurse to join the clinical research team as Protocol Coordinator. The role requires independent work, collaboration with physicians, patients, data managers, and hospital staff, and adherence to hospital policies.

Responsibilities include protocol review, patient eligibility, informed consent, data entry, SAE reporting, and training other coordinators.