We are looking for a skilled Senior Clinical SAS Programmer with a strong background in the Oncology therapeutic area to support our clinical development programs. The ideal candidate will have at least 3 years of hands-on experience working with SDTM, ADaM, and TLF (Tables, Listings, and Figures), along with a solid understanding of clinical trial data and CDISC standards.

Key Responsibilities:

• Develop, validate, and maintain SAS programs to support the generation of SDTM and ADaM datasets according to CDISC guidelines
• Create and validate Tables, Listings, and Figures (TLFs) for clinical study reports and regulatory submissions
• Work collaboratively with statisticians, clinical data managers, and other team members
• Ensure high-quality, accurate, and timely deliverables
• Support multiple oncology studies across various phases (Phase I–III)
• Review and contribute to programming specifications and documentation
• Assist in submission activities including the preparation of define.xml and reviewer’s guides

Qualifications:

• Bachelor’s or Master’s degree in Statistics, Computer Science, Life Sciences, or a related field
• At least 3 years of experience as a clinical SAS programmer in the pharmaceutical, biotech, or CRO industry
• Solid experience in oncology clinical trials
• Strong knowledge of CDISC SDTM and ADaM standards
• Hands-on experience creating and validating TLFs
• Working knowledge of clinical trial processes and regulatory requirements
• Effective communication and collaboration skills
• Strong attention to detail and problem-solving abilities

If you are a driven professional seeking to make a meaningful impact in clinical research, we encourage you to apply. Please send your CV to [email protected].