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!