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We are the makers of possible. BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. The Senior Clinical Database Programmer is responsible for ensuring that clinical study data is collected, processed, and validated in a consistent and appropriate manner that is consistent with BD's QMS procedures, resulting in high quality data ready for statistical analysis. They are responsible for all end-to-end clinical data management programming activities for assigned studies. This role provides clinical data management programming leadership within the study team to align on and drive data collection requirements for one or more studies. The programmer efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects. They also establish and maintain productive working relationships with other functional areas that contribute to the execution of clinical studies, enforce data standard conventions and quality expectations for clinical data per defined processes, and review and provide input on data management related study documents and plans. The Senior Clinical Database Programmer creates and develops clinical databases and data transfer files according to written specifications, develops and evaluates database configurations, including edit checks, derivations, and form/field dynamics. They utilize SQL/SAS to create and test reports and listings, ensuring data consistency and facilitating data review. The role also involves handling pre-processing and loading of non-CRF data files, collaborating with IT to address routine technical problems and solutions, and acting as a technical resource to other members of the team. The programmer plans appropriately to ensure adherence to study timelines and leads/provides the relevant support and input to continuous improvement activities within clinical data management.
