Statistical Programmer

Company Description Gurus CRO is the first and largest biometrics-focused contract research organization in Armenia, partnering with global biotech and pharmaceutical companies that rely on its technical expertise and commitment to data integrity. The company provides end-to-end biometrics services for all phases of clinical trials, including clinical data management, statistical programming in SAS and R, biostatistics, and project management. Its certified programmers, experienced biostatisticians, and dedicated data managers deliver high-quality, CDISC-compliant outputs that align with international regulatory standards. By turning complex data into reliable evidence, Gurus CRO helps sponsors move through clinical development with greater speed, confidence, and clarity.

Role Description: This is a full-time, on-site Statistical Programmer role based in Yerevan/Vanadzor/Ijevan/Gyumri/Tbilisi. The Statistical Programmer will produce, validate, and maintain analysis datasets, tables, listings, and figures for clinical trials using SAS and/or R in accordance with CDISC and regulatory requirements. Daily activities include writing and reviewing programming specifications, developing and optimizing reusable macros, and ensuring consistency between raw data, derived datasets, and statistical outputs. The role involves close collaboration with biostatisticians, data managers, and project managers to clarify requirements, resolve data or programming issues, and support study timelines. The Statistical Programmer will also contribute to documentation, quality control, and process improvement initiatives within the biometrics team.

Qualifications

• Strong skills in Statistical Programming and general Programming for clinical trial data analysis.
• Solid understanding of Statistics and applied statistical concepts used in clinical research.
• Experience with Data Management concepts, including handling clinical trial datasets and ensuring data quality.
• Proficiency in developing and maintaining Macro code to streamline and standardize programming tasks.
• Bachelor’s or master’s degree in biostatistics, statistics, computer science, mathematics, life sciences, or a related field.
• Experience with SAS and/or R in a clinical, pharmaceutical, or CRO environment; familiarity with CDISC SDTM and ADaM standards is highly desirable.
• Understanding of ICH-GCP and regulatory requirements (e.g., FDA, EMA) relevant to clinical trial programming.
• Strong analytical thinking, attention to detail, and problem-solving skills, with the ability to document work clearly and reproducibly.
• Effective communication skills and ability to collaborate in cross-functional teams in a fast-paced environment.
• Ability to manage multiple tasks, prioritize effectively, and meet project deadlines.