Clinical Monitor - University of Southern California

San Diego, CA

Job Description: Clinical Research Coordinator

Responsibilities:

Coordinate clinical trials in compliance with site operating procedures and ICH guidelines.

Ensure adherence to Title 21 CFR Part 11, FDA, IRB, and HIPAA regulations.

Manage study documentation and electronic data capture systems.

Facilitate FDA audits and maintain Good Clinical Practices.

Communicate effectively using medical terminology.

Qualifications:

Bachelor's degree in life sciences or related field.

Experience in clinical research coordination.

Strong knowledge of drug development and clinical trial regulations.

Proficiency in electronic data management systems.

Source : University of Southern California