--- title: Statistical Programmer – All Levels (Junior to Senior) at Gurus CRO description: Company Description 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 --- # Statistical Programmer – All Levels (Junior to Senior) **Company:** Gurus CRO **Location:** Tbilisi, Georgia **Posted:** 2026-10-17 **Apply by:** 2026-12-01 [Apply / View original posting](https://www.linkedin.com/jobs/view/4476448007) ## Job description Company Description 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 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. Role Description 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 Qualifications Junior level 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 Mid-level 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 Senior level 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 Core Competences 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 Why Join Gurus 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 Apply via LinkedIn or send your CV to: hr@gurus.am --- 🔔 [Monitor similar jobs on Gurify](https://gurify.com/?utm_source=techgeo&utm_medium=jobboard&utm_campaign=monitor_similar&role=Statistical+Programmer+%E2%80%93+All+Levels+%28Junior+to+Senior%29) — get alerted when matching roles are posted in Georgia. ```json {"@context":"https://schema.org/","@type":"JobPosting","title":"Statistical Programmer – All Levels (Junior to Senior)","description":"

Company Description 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 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. Role Description 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 Qualifications Junior level 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 Mid-level 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 Senior level 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 Core Competences 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 Why Join Gurus 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 Apply via LinkedIn or send your CV to: hr@gurus.am

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