Senior Statistical Programmer - Remote (US)
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?
MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains an industry‑leading customer satisfaction rating and fosters a collaborative and inclusive work environment where employees can thrive.
Join us at MMS and be part of a team that is shaping the future of clinical research.
- Mastery and training on generating tables, listings, and graphs from clinical trial databases using SAS
- Utilizes System Development Life Cycle (SDLC) for programming deliverables
- Advanced user in SAS programming, SAS Base, and SAS Macros
- Advanced knowledge of E‑Submission Standards, Guidelines and Regulations
- Mastery and training on SDTM standards including ability to write specifications
- Advanced knowledge of ADaM standards including supporting specification writing
- Proficient with MS Office applications
- Advanced knowledge of ICH, 21
CRF Part 11, and ISO 9001:2000 requirements - Advanced experience with pooling of data sets for submissions
- Advanced experience with BIMO outputs, define.xml, Reviewer's Guides, SDSP
- Lead study or small programming project teams
- Masters required for all Statistics roles
- Minimum of 5 years’ experience in Statistical Programming or similar field required
- Expert knowledge of scientific principles and concepts
- Reputation as emerging leader in field with sustained performance and accomplishment
- Proficiency with MS Office applications
- Hands‑on experience with clinical trial and pharmaceutical development preferred
- Good communication skills and willingness to work with others to clearly understand needs and solve problems
- Excellent problem‑solving skills
- Good organizational and communication skills
- Familiarity with current ISO 9001 and ISO 27001 standards preferred
- Familiarity with 21 CFR Part 11, FDA, and GCP requirements
- Basic understanding of CROs and scientific & clinical data/terminology, and the drug development process
- Mid‑Senior level
- Full‑time
- Sales, General Business, and Education
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