Clinical Data Analyst

Key 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

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