Gurus CRO

Statistical programmer in clinical trials

In short

Statistical Programmer role at GURUS CRO, developing and validating SAS/R programs, SDTM/ADaM datasets, and TLFs for clinical trial data in a GxP-regulated environment, working closely with Biostatistics and Data Management teams. The company is a CRO serving global biotech and pharmaceutical clients. Requires a degree in Statistics, Mathematics, Computer Science or related field, SAS/R programming skills, CDISC standards experience, and 4+ years in clinical trial statistical programming for senior candidates, including mentoring and leading programming activities. Office-based in Tbilisi, full-time.

About the Role
GURUS CRO, a trusted partner for global biotech and pharmaceutical companies, recognized for its technical expertise, precision, and commitment to data integrity, is expanding its biometrics team. We are looking for Statistical Programmers (Junior to Senior levels) to join our biometrics team. In this role, you will contribute to the development of high-quality statistical deliverables for clinical trials in a GxP-regulated environment, working closely with Biostatistics and Data Management teams.
Responsibilities
•Develop, validate, and maintain SAS and/or R programs for clinical trial data analysis
•Generate and validate SDTM and ADaM datasets, Tables, Listings, and Figures (TLFs)
•Ensure full compliance with CDISC standards and regulatory submission requirements
•Perform data validation, quality control, and documentation in line with internal and external standards
•Collaborate with cross-functional teams to support clinical study deliverables
•Contribute to process optimization, standardization, and continuous improvement initiatives
•Participate in code reviews and quality assurance activities
Requirements
•Bachelor's degree in Statistics, Mathematics, Computer Science, or a related discipline
•Foundational knowledge of SAS or R programming
•Strong analytical thinking and attention to detail
•2–4 years of experience in statistical programming within clinical research or related field
•Practical experience with CDISC standards (SDTM/ADaM)
•Solid understanding of clinical trial data structures and workflows
•4+ years of experience in clinical trial statistical programming
•Advanced proficiency in SAS
•Experience leading programming activities and mentoring junior team members
•Strong knowledge of regulatory submission processes and standards
•Strong attention to detail and data accuracy
•In-depth understanding of GxP and clinical research standards
•Analytical mindset with strong problem-solving capabilities
•Effective communication skills in English (written and verbal)
•Ability to operate in a collaborative, high-performance environment
Conditions
•Be part of a growing organization with a strong commitment to quality
•Work in a professional, collaborative, and high-standard environment
•Opportunity to contribute to impactful projects and continuous improvement initiatives

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