Associate Director, Clinical Data Management

Role: Associate Director, Clinical Data Management at RayzeBio, overseeing data integrity across multiple oncology clinical trials. Responsibilities include leading data management activities, managing CRO relationships, ensuring data quality and compliance with GCP, CDISC/CDASH standards, and FDA regulations, and contributing to SOP development. The role involves hands-on oversight of data collection, validation, and analysis within clinical systems such as EDC (Medidata RAVE/Veeva), IVRS, and CTMS, with a focus on oncology indications. Qualifications: Bachelor's degree in Life Sciences or related field; minimum of 6 years in clinical data management within pharma/biotech/CRO sectors; extensive experience with clinical systems, data standards, and GxP. Preferred: oncology therapeutic area expertise, strong vendor management skills, and knowledge of regulatory compliance. The role requires cross-functional collaboration with clinical operations, biostatistics, and external vendors, with 10% travel. Position is remote in the U.S.