• 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.