SAS Programmer

Katalyst HealthCares and Life Sciences

• $100K — $130K *
San Francisco, CA 94112In-Person
Pharmaceuticals & Biotech
5 - 7 years of experience
Today
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Job Overview by Ladders

Qualifications

  • 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.

Responsibilities

  • Develop, maintain, and execute SAS programs for external data transfers and validation.
  • Generate and maintain Data Review Listings (DRLs) and Study Health Metrics (SHMs) per study timelines.
  • Perform peer reviews of DRLs and data reconciliation reports.
  • Monitor and troubleshoot automated job logs.
  • Retrieve and post external vendor data using sFTP/FTP clients.
  • Collaborate with data teams to ensure data integrity and cleaning activities.
  • Contribute to SAS macro program development and departmental standards.
  • Assist in SOP and work instruction development, including program validation.

Benefits

  • Opportunities for professional development and growth.
  • Collaborative work environment with cross-functional teams.
  • Exposure to cutting-edge oncology studies and protocols.
  • Ability to mentor and guide junior programming staff.
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.
* Ladders Estimates

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