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 a 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 our proven, scientific approach to complex trial data and regulatory submission challenges. With a integral footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also 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.
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We are looking for a full-time employee, remotely based within any location in Mexico.
Job Specific Skills
Mastery and trained 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 trained 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, 21CRF Part 11, and ISO ****:**** 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
Job Requirements
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 **** and ISO ***** standards preferred.
Familiarity with 21 CFR Part 11, FDA, and GCP requirements
Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.
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📌 Senior Statistical Programmer (Remote - Mexico) (México)
🏢 MMS
📍 México