Lead Statistician

We are seeking a highly skilled Statistical Programmer to join our team.

The Senior Statistical Programmer provides lead statistical programming support for multiple clinical projects using SAS and provides expert consultation across the company. Key responsibilities include delivering key regulatory-compliant output, developing programming documentation, writing efficient code, staying updated on programming techniques, and mentoring staff.

• Provides lead statistical programming support for multiple clinical research study projects or study teams.
• Develops programming documentation and annotations including specifications, review of mock shells, adhering to relevant Standard Operating Procedures and may contribute to standardization efforts.
• Writes well-documented, efficient, and high-quality code, conducts code review, supports cross-functional programming activities, and programming validation as needed.
• Presents statistical programming topics internally and may present at external conferences.

• A bachelor's degree plus 4 years Statistical programming experience as a CDISC/TLF Statistical programmer in Pharmaceutical/CRO environment, education in a scientific discipline preferred.
• Understanding of GCP principles and other regulatory standards (e.g. FDA, EMA, and ICH guidance and recommendations) in Clinical Research.
• Good analytical skills with the ability to process scientific and medical data.
• Strong statistical programming skills in SAS, familiarity with R, Python or other relevant statistical software considered beneficial.

This role offers opportunities for professional growth and development, working on complex clinical projects and collaborating with experienced professionals in the field.