R/SAS Statistical Programmer (hiring in Armenia, Hungary, Estonia, CR, Romania, Argentina, Brazil, or Columbia only) Updated: YesterdayLocation: Bogota, DC, ColombiaJob ID: -OTHLOC-7352-2DR We are seeking an R/SAS Statistical Programmer to build, validate and run custom programming code that generates summary tables, listings, graphs and derived datasets as specified in statistical analysis plans and programming specifications. The candidate will work closely with biostatisticians and project teams to ensure high‑quality outputs and timely delivery across multiple concurrent projects. Job Responsibilities MUST BE LOCATED IN ONE OF THE FOLLOWING LOCATIONS WITH NO SPONSORSHIP NEEDS: Armenia, Hungary, Estonia, CR, Romania, Argentina, Brazil, or Columbia R and SAS Programming experience required CDISC - SDTM/ADAM programming experience required Use R and SAS to develop custom code for summary tables, data listings, graphs, and derived datasets. Perform validation programming and collaborate with programmers, biostatisticians, and other team members to resolve discrepancies. Keep project team members informed of programming progress and issues requiring attention. Follow applicable SOPs, WIs, and regulatory guidelines (e.g., ICH). Maintain well‑organized, complete, and up‑to‑date project documentation and quality‑control documents to ensure inspection readiness. Manage scheduling and time constraints across multiple projects, setting goals, and adapting to changes. Develop specifications for datasets and outputs of any complexity according to statistical or sponsor requirements. Conduct effective internal meetings, distribute relevant information, and follow action items to completion. Assist with projects and initiatives as required, ensuring on‑time delivery and risk mitigation. Act as the lead statistical programmer, directing programming activities and monitoring progress. Review project documentation such as Statistical Analysis Plans, mock shells, and programming specifications, providing constructive feedback. Participate in sponsor meetings, kickoff meetings, and bid defense meetings as the statistical programming representative. Mentor programming personnel through training courses, presentations, and guided reviews. Maintain a strong understanding of clinical drug development, industry standards, and electronic submission requirements. Collaborate with biostatistics and statistical programming personnel to develop SOPs, guidelines, and procedures. Contribute to programming tools and macros for standardization and efficiency. Provide guidance on CDISC Standards and perform compliance reviews of deliverables such as SDTM, ADaM, and DEFINE.XML. Participate in industry standards organizations and update the Biometrics Department on regulatory changes. Transfer deliverables and perform other work‑related duties as assigned. Qualifications Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of a degree, an equivalent combination of education and demonstrated programming experience. Extensive programming experience in R or other required software, preferably in a clinical trial environment. Knowledge and experience in the use of CDISC Standards for regulatory agency requirements; experience in submissions to regulatory agencies preferred. Experience in mentoring others in clinical trial processes and CDISC Standards. Excellent written and verbal communication skills. Ability to read, write, speak, and understand English. Equal Opportunity Employment Syneos Health is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants in performing the essential functions of the job as well as to maintain compliance with the legislation of each country in which it operates. #J-18808-Ljbffr