Senior Statistical Programmer

Senior Statistical Programmer
Work Schedule: Monday–Friday, 40 hours per week
Monthly Compensation: USD $4,000–$8,000, depending on experience and qualifications, based on 40 hours per week
Industry: Clinical Research | Pharmaceuticals | Biotechnology
Recruiting Partner: OttoMate
About the Role
Turn complex clinical trial data into reliable insights that support drug development and regulatory submissions.
OttoMate is recruiting a Senior Statistical Programmer on behalf of a confidential client providing data analytics and clinical programming solutions to the pharmaceutical and healthcare sectors.
This opportunity is ideal for an experienced programmer who enjoys taking ownership of complex deliverables, collaborating with biostatisticians, and maintaining the rigorous quality standards that clinical research demands.
You will apply your expertise in SAS, CDISC, SDTM, ADaM, and tables, listings, and figures (TLFs) to produce accurate, traceable, submission-ready outputs. You will also help strengthen programming practices and mentor colleagues while contributing to meaningful clinical programs.
The client’s identity will be shared during your introductory interview with OttoMate.
Required Qualifications
8+ years of relevant statistical programming experience within the pharmaceutical, biotechnology, CRO, or clinical research industry.
Bachelor’s degree in Statistics, Biostatistics, Mathematics, or a directly related quantitative field. This is a mandatory requirement.
Advanced proficiency in SAS, including the development and independent validation of production-quality clinical programs.
Hands-on experience creating SDTM and ADaM datasets and producing TLFs.
Strong understanding of CDISC standards, clinical trial methodology, and statistical analysis workflows.
Experience with clinical data validation, quality-control procedures, and clinical data management processes.
Demonstrated ability to deliver senior-level programming work independently and with limited supervision.
Strong analytical judgment, problem-solving skills, and attention to detail.
Strong written and spoken English for collaboration with international teams.
Why Consider This Opportunity?
Apply your expertise to meaningful clinical research: contribute to analyses supporting drug development and evidence-based decisions.
Own challenging technical work: develop and validate complex clinical datasets and outputs.
Broaden your contribution: participate in submission support, programming standards, and process improvement.
Share your expertise: mentor junior programmers and strengthen team capability.
Collaborate across disciplines: work with biostatisticians, clinical data managers, and other clinical research professionals.
How to Apply
Interested? Please apply directly through this LinkedIn job posting and submit your updated CV in English.
If you have any questions, feel free to contact Fernando Leon:
LinkedIn: linkedin.com/in/fernandoleonmx
Email: fernando@ottomate.global
Please mention “Senior Statistical Programmer (SAS)” when reaching out.
Ottomate is proud to be an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all team members, regardless of race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other characteristic protected by applicable law."

Work arrangement
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