Senior Clinical & Statistical Programmer

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Clinical & Statistical Programmer based in the United States.
The Senior Clinical & Statistical Programmer will play a key role in advancing clinical development programs by delivering accurate, high-quality statistical programming outputs throughout the clinical trial lifecycle. This hands-on position combines advanced SAS expertise with oversight of external programming partners and a strong focus on data integrity and regulatory compliance. You will develop and validate clinical datasets, tables, listings, and figures while supporting clinical study execution and regulatory submissions. Working closely with cross-functional teams, you will help ensure that programming deliverables meet CDISC standards and applicable regulatory requirements. The role offers the opportunity to contribute to evolving programming standards, improve processes, and support innovative therapies in a collaborative biotechnology environment. The position is open to remote candidates across the United States, with a preference for candidates able to work from the Seattle office at least two days per week.

Skills
Regulatory Compliance

Experience
5+ yrs

Employment type
Full-time

Work arrangement
Yes