At a Glance
- Tasks: Lead programming teams to generate insightful data from clinical trials using SAS.
- Company: MMS, a data-driven clinical research organisation in the UK.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Join a dynamic team focused on impactful clinical research.
- Why this job: Make a real difference in drug development while leading innovative projects.
- Qualifications: 5+ years in statistical programming with expertise in drug development and regulatory submissions.
The predicted salary is between 50000 - 70000 £ per year.
MMS is a data-focused clinical research organization seeking an experienced SAS Programmer in the United Kingdom.
The role involves generating tables, listings and graphs from trial databases using SAS, applying the SDLC framework, and leading small programming teams.
Qualified candidates have 5+ years in statistical programming, expert understanding of drug development and regulatory submissions, and strong MS Office skills.
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We think you need these skills to ace Senior SAS Programmer — Lead Clinical Trial Data in Telford
SAS Programming
Statistical Programming
SDLC Framework
Data Analysis
Drug Development Knowledge
Regulatory Submissions Knowledge
Team Leadership
