Clinical Quality Control Associate II

Conduct quality control reviews of clinical trial data in compliance with study protocols, Good Clinical Practices, and Standard Operating Procedures. Record, track, and ensure resolution of data queries while documenting or reporting clinical trial deviations and identifying error trends. Assist in sponsor and regulatory audits, maintain computerized files, and compile data for timed study events. Mentor Quality Systems team members, provide feedback for performance reviews, and proactively communicate issue resolutions to supervisors. Maintain confidentiality of participants and sponsors while advocating for high-quality customer service within the department.