Senior Manager, Clinical Data Management

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/ RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals The Senior Manager, Clinical Data Management, will play a crucial role in our data management efforts, ensuring the accuracy, consistency, and integrity of clinical data. This position will provide oversight of data management activities, from planning and coordination to execution and quality control. The successful candidate will be responsible for managing relationships with external partners and collaborating across cross-functional teams to ensure data deliverables and expectations are met. Job Responsibilities * May simultaneously function as lead Clinical Data Manger for multiple clinical trials. * Coordinates day-to-day data management study tasks including reviewing data management documents to ensure a consistent approach. * Review project timelines and metrics to ensure databases are delivered on schedule. * Responsible for ensuring the data collected meets the requirements of the study objective and company quality standards. * Engage in cross-functional meetings, providing updates on project status, issues, and milestones. * Provide oversight of data management personnel and activities of CROs and vendors. * Lead interactions with third party vendors (e.g., laboratories) on collection, transmittal, and transfer of study specific data. * Review data using listings and visualization tools to support performance and quality reporting; conduct study-level reviews to identify trends. * Experience with clinical systems including EDC, IVRS, CTMS, eTMF, and other clinical project management tools; ability to learn new systems as needed. * Supports the development, review and implementation of processes, policies, standard operating procedures (SOPs) and associated documents affecting data management. * Regularly utilize AI tools to enhance productivity and discover potential new ways to optimize team workflows and processes. * Experience with clinical systems including EDC, IVRS, CTMS, eTMF, and other clinical project management tools; ability to learn new systems as needed. * Applies AI to improve team execution and decision‑making Education and Experience * Bachelor’s degree in Life Science, mathematics, or health-related fields preferred. * Minimum of 4 years data management experience in pharmaceutical/biotech/CRO industry; extensive hands-on experience in all aspects of data management. * Experience with clinical systems including EDC, IVRS, CTMS, eTMF, and other clinical project management tools * Experience in the Oncology therapeutic area is preferred. * Proven ability to manage CRO relationships and oversee data management deliverables. * Strong knowledge and experience of EDC systems (Veeva preferred). * Solid knowledge of GCP, CDISC/CDASH data structures, ICH guidelines and FDA regulations. * Excellent verbal and written communication...