Temp Statistical Programmer

Requirements:

• A BS/BA, MS, or other relevant qualification.
• At least 8–12 years of statistical programming experience with clinical trial data using SAS; industry experience is essential.
• Strong written and verbal communication skills.
• Ability to manage multiple priorities, anticipate challenges, and achieve goals as part of an interdisciplinary team.
• Oncology experience is preferred.
• A record of teamwork, adaptability, and enthusiasm for adopting or applying innovative approaches and technologies in a collaborative, fast-paced environment is preferred.

Responsibilities:

• Provide statistical programming support by producing or verifying SAS scripts and outputs for analysis files, tables, listings, figures, and other clinical trial deliverables.
• Write analysis file specifications and other documentation describing deliverables and analysis methods.
• Plan work to support timely delivery and meet quality standards.
• Follow project and study programming standards, specifications, and internal guidelines.
• Perform biometrics quality control of clinical-data documents to help ensure accurate results for internal and external audiences.
• Support deliverables such as investigator brochures, publications, US and ex-US regulatory submissions, CDISC-compliant SDTM and ADaM datasets, data documentation, Reviewers Guides, tables, listings, figures, and study-specific and integrated statistical analysis plans.
• Program in-house deliverables, including materials for dose committee and board of director meetings and exploratory analyses.
• Review statistical analysis plans, documents, spreadsheets, and slides prepared for internal presentations and external publications.
• Work closely and communicate effectively with statisticians, internal colleagues, and members of other functional groups to meet deliverable needs and study timelines.

Technologies:

• Support
• SAS
• SAP

More

We are hiring a Statistical Programmer for a six-month assignment, with a possible extension, based in Redwood City, California, on a hybrid schedule. The role supports clinical trial programming and verification in a fast-paced environment.

last updated 43 week of 2026