Join MMS, a Great Place to Work certified organization, as a Senior Statistical Programmer to contribute to shaping the future of clinical research. With a global footprint and industry-leading customer satisfaction rating, MMS offers a collaborative and inclusive work environment where employees can thrive.
Requirements
- Mastery in generating tables, listings, and graphs from clinical trial databases using SAS
- Advanced user in SAS programming, SAS Base, and SAS Macros
- Advanced knowledge of E-Submission Standards, Guidelines and Regulations
- Mastery and train on SDTM standards including ability to write specifications
- Proficient with MS Office applications
- Advance knowledge of ICH, 21CRF Part 11, and ISO 9001:2000 requirements
- Lead study or small programming project teams
- Independently manages tasks and projects to achieve set objectives
Benefits
- Award-winning, data-focused clinical research organization (CRO)
- Great Place to Work certified organization
- Industry-leading customer satisfaction rating
- Collaborative and inclusive work environment
To apply for this job please visit mmsholdingsinc.applytojob.com.

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