Principal Statistician

We are seeking a skilled and experienced Senior Statistical Programmer to join our team. As a key member of our research support group, you will provide lead statistical programming support for multiple clinical projects using SAS.

• Deliver high-quality output that meets regulatory requirements
• Develop and maintain programming documentation and annotations
• Write efficient and well-documented code

To succeed in this role, you will need to have a strong understanding of statistical programming principles and experience working with SAS. You will also need to be able to analyze data and identify trends, as well as communicate effectively with cross-functional teams.

We offer a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and detail-oriented individual who is passionate about statistical programming, we encourage you to apply.

• Bachelor's degree in a scientific discipline
• At least 4 years of experience as a CDISC/TLF Statistical Programmer in a Pharmaceutical/CRO environment
• Understanding of GCP principles and other regulatory standards (e.g. FDA, EMA, ICH)
• Strong analytical skills and ability to process scientific and medical data
• Proficiency in SAS and familiarity with R, Python or other relevant statistical software