Senior Programmer Submission

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Senior Programmer Submission based in the United States. The Senior Programmer Submission combines hands-on statistical programming expertise with technical leadership across clinical trial studies and regulatory submissions. In this role, you will lead programming activities, ensure the accuracy and quality of clinical datasets and outputs, and support the delivery of compliant submission packages. You will work closely with study statisticians, project managers, and programming teams to coordinate resources, manage deliverables, and resolve technical challenges. The position requires strong knowledge of CDISC standards, SAS programming, and regulatory requirements, with a focus on maintaining high-quality, consistent programming practices. You will also contribute to process improvement, technical training, and the development of reusable programming solutions. This is an opportunity to make a meaningful contribution to clinical research within a collaborative, quality-driven environment.