Associate Director, Clinical Data Management

Role: Associate Director, Clinical Data Management at Corcept, focusing on optimizing data collection, flow, and access across clinical trial databases, ensuring accuracy, completeness, and CDISC compliance. Responsibilities: oversee vendor selection and management for data activities, lead design of data flow infrastructure across EDC and non-EDC sources, develop real-time data access processes, review data quality and query resolution, manage SAE reconciliation, and support audits. Qualifications: Master’s degree in life sciences preferred; 10+ years in clinical trial data management within pharma, biotech, or med device; experience with MedDRA, WHODrug, CDISC/SDTM, and mainstream EDC systems (e.g., Rave, Medrio). Skills: SQL, SAS, relational databases, data visualization tools (Spotfire, Tableau), and regulatory compliance (ICH, GxP, 21CFR Part 11). Preferred: experience with endocrinology trials, biomarker data curation, and CRO oversight. High-Value: clinical data management leadership in biotech/pharma, experience with regulatory audits, and expertise in clinical trial IT systems. Work Setup: headquarters-based in Redwood City, California.