Clinical QC Manager- Hybrid

Clinical QC Manager based in South San Francisco (hybrid) responsible for conducting independent QC assessments of investigational sites to ensure adherence to study protocols, GCP, and company procedures. Collaborates with CTMs, CRAs, and Clinical Operations staff to identify protocol adherence gaps, recurring operational issues, and process risks; develops QC plans, tools, and reports, and supports inspection readiness. Performs risk-based on-site QC visits, reviews essential documents and safety reporting processes, escalates significant concerns, contributes to RCA/CAPA, and participates in cross-site trend analysis. Requires a Bachelor’s degree in medical science or related field and five years of clinical research experience with quality-related activities; prefers deep knowledge of clinical trial processes, ICH-GCP, and effective communication skills. The role includes frequent travel to investigational sites and is based in the U.S. with a hybrid work arrangement.