Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

SAS Programmer

Job

Katalyst Healthcares & Life Sciences

San Francisco, CA (In Person)

Full-Time

Posted 1 week ago (Updated 1 week ago) • Actively hiring

Expires 7/14/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
74
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

SAS Programmer Katalyst Healthcares & Life Sciences - 4.0 San Francisco, CA Job Details Contract 1 hour ago Qualifications SFTP Crystal Reports
SAS FDA 21 CFR
Part 11 SAS language ICH guidelines CDISC standards Clinical quality assurance standards Oncology Statistical analysis tools
Full Job Description Responsibilities:
Develop, maintain, and execute SAS programs to support external data transfers, including validation against vendor transfer specifications. Generate and maintain Data Review Listings (DRLs) and Study Health Metrics (SHMs) in accordance with study timelines. Perform peer review of DRLs and data reconciliation reports. Monitor automated job logs and resolve issues as needed. Retrieve and post external vendor data using sFTP/FTP clients and vendor portals. Collaborate with data managers, statistical programmers, biostatistics, and clinical operations to support data cleaning and integrity activities. Contribute to the development and maintenance of SAS macro programs and departmental programming standards. Participate in SOP and work instruction development, including program validation and documentation. Provide guidance and support to junior members of the data programming team.
Requirements:
Bachelor's or Master's degree in a relevant field or equivalent experience. 7+ years of clinical data programming experience, with a minimum of 5 years in oncology. Hands-on experience across Phase I, II, and III oncology trials. Proficiency in SAS; working knowledge of Medidata Rave, Business Objects, and Crystal Reports. Familiarity with
CDISC, 21 CFR
Part 11, ICH, and GCP guidelines. Experience with sFTP/FTP tools and vendor data portals.