Senior Statistical Programmer

Contact name: Emily Munn

Contact email:
Job ref: 573
Published: about 2 months ago
A leading provider of innovative solutions for rare disease research and development, is seeking a seeking a talented Senior Statistical Programmer with a strong background in clinical trial data analysis to join their team on a contract basis.

In this role, you will be responsible for supporting the statistical analysis of clinical trial data, writing and maintaining SAS programs, and working closely with our biostatistics team to ensure the delivery of high-quality results.

About you:
  • A Bachelor's or Master's degree in a relevant field (e.g., statistics, mathematics, computer science).
  • A minimum of 3 years of experience in SAS programming in the pharmaceutical industry.

The responsibilities:
  • Design, develop, and maintain SAS programs for the analysis of clinical trial data
  • Work closely with the biostatistics team to ensure the delivery of high-quality results
  • Support the analysis of data from clinical trials and other studies
  • Write and review program validation documents and study reports
  • Collaborate with cross-functional teams, including data management, clinical operations, and regulatory affairs

This client offers a competitive salary and benefits package, as well as a dynamic and supportive work environment. If you're passionate about making a difference in the lives of patients with rare diseases, and have the skills and experience we're looking for, we want to hear from you!