Statistical Programmer

14405Contract Competitive Fully Remote Fully Remote - United Kingdom Updated on: 17-03-2025

We are currently looking for a Safety Statistical Programmer to join a leading pharmaceutical company on a remote basis. As the Safety Statistical Programmer, you will be responsible for contributing to the creation and delivery of safety analyses and reports to support pharmacovigilance activities.

KEY DUTIES AND RESPONSIBILITIES:

1. Perform SAS programming (Base SAS, SAS/STAT, SAS Macro) and R for safety data analysis.
2. Collaborate closely with safety statisticians to ensure specifications for safety analyses are complete and statistical plans are executed efficiently with the right level of validation.
3. Provide programming support for Safety Assessment Committees (SAC) and Safety Management Teams (SMT) meetings, including the timely generation of ad-hoc analyses and tables, listings, figures (TLFs).
4. Compute background rates from various sources for key adverse events of safety interest and implement statistical methods for safety monitoring in blinded clinical trials.

ROLE REQUIREMENTS:

1. Relevant degree in statistics, mathematics, or a related field.
2. Proven industry experience in programming within the pharmaceutical industry.
3. A working knowledge and practical experience with SAS programming (Base SAS, SAS/STAT, SAS Macro) and R for safety data analysis.

Key Words: Safety Statistical Programmer / pharmacovigilance / safety analysis / SAS programming / R programming / clinical trials / safety data / statistical programming / adverse events / regulatory submissions