Looking for a Senior SAS Programmer to join a leading biotech company developing cutting-edge drugs for life-changing brain diseases including Parkinson's. 

Role

• Develop SAS programs which generate datasets, complex listings, tables and complex graphs.
• Able to Generate SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files
• Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs
• You'll be overseeing deliverables for multiple clinical studies to ensure high quality and meet the pre-specified timelines
• Support the preparation of clinical study reports, regulatory submissions, publications, annual DSUR, and exploratory analyses.
• Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions.

Experience

• 10+ years of experience as a Statistical Programmer in a Biotech/Pharma OR CRO environment supporting drug development, medical device development, or intervention studies.
• Exceptional SAS programming skills and expertise in the development and implementation of statistical programming procedures and processes in a clinical development environment
• Proven experience with CDISC standards (SDTM, ADaM, and Define.xml), medical terminology, clinical trial methodologies, and FDA/ICH regulation
• Experience supporting regulatory submissions, and interacting with the global regulatory authorities.
• Excellent communication skills and ability to work with international stakeholders as part of a global team

If you're looking for your next challenge please apply now.

You'll need to be based in the US already for this role as well as the right to work.