Assoc Director, Statistical Programming
Job Description
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an Associate Director, Statistical Programming based in the United States.
This senior-level role is central to the delivery of high-quality statistical programming outputs that support global clinical development and regulatory submissions. You will lead and oversee programming activities that generate analysis datasets, tables, listings, and figures used in clinical study reports and integrated summaries. The position requires deep expertise in clinical trial reporting processes, regulatory standards, and advanced statistical programming within a highly regulated biopharmaceutical environment. You will collaborate closely with clinical development teams, biostatistics, and cross-functional stakeholders to ensure timely and accurate deliverables. The role involves both strategic oversight and hands-on technical leadership across complex, time-sensitive studies. You will also contribute to process improvements, resource planning, and harmonization of programming standards across therapeutic areas. This is a high-impact position where your work directly supports regulatory approvals and the advancement of life-changing therapies.
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an Associate Director, Statistical Programming based in the United States.
This senior-level role is central to the delivery of high-quality statistical programming outputs that support global clinical development and regulatory submissions. You will lead and oversee programming activities that generate analysis datasets, tables, listings, and figures used in clinical study reports and integrated summaries. The position requires deep expertise in clinical trial reporting processes, regulatory standards, and advanced statistical programming within a highly regulated biopharmaceutical environment. You will collaborate closely with clinical development teams, biostatistics, and cross-functional stakeholders to ensure timely and accurate deliverables. The role involves both strategic oversight and hands-on technical leadership across complex, time-sensitive studies. You will also contribute to process improvements, resource planning, and harmonization of programming standards across therapeutic areas. This is a high-impact position where your work directly supports regulatory approvals and the advancement of life-changing therapies.