
This full-time Senior Statistical Programmer role supports clinical trial data analysis and regulatory submissions within the ACI Clinical organization. The position involves developing, validating, and documenting SAS programs for datasets and outputs, while leading programming activities and managing project timelines. Key responsibilities include conducting quality control checks, mentoring junior staff, and collaborating with cross-functional teams to ensure compliance with industry standards. The role offers remote flexibility and provides opportunities for professional growth through mentorship, certification assistance, and a supportive culture that values employee development and work-life balance.







