Junior Statistical Sas Programmer

The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures, and listings for clinical studies (according to ICH E3), publications, or Health Authorities requests. Collaborates with Biostatistics and Data Management staff on clinical trials/projects. Some of what you'll do : Develop SAS programs for generating datasets, tables, figures, and listings for clinical trials (according to ICH E3), publications, and Health Authorities requests. Use CDISC guidelines to generate SDTM / ADaM datasets. Write Programming Specifications of analysis datasets. Validate ADaM datasets using Pinnacle 21. Prepare, maintain, and archive CDISC documentation for ADaM (Define.xml and ADRG). Contribute to developing standard SAS macros and prepare corresponding validation documents. Liaise with Data Management team and develop SAS programs/macros/utilities to detect data discrepancies. Check requirements to handle external clinical data and develop SAS programs to import/reconcile external clinical data. Develop and validate SAS programs for identification of Non-Protocol Deviations. Collaborate with Biostatistics and Data Management staff on clinical trials/projects. Maintain and archive SAS programming documentation. Establish and maintain SOPs and templates related to Statistical SAS programming. Stay informed on new SAS developments relevant to clinical trial data management. Ensure KPIs and metrics for assigned studies are met. Complete required trainings on time. Perform daily entries in the TRACK system, including billable and non-billable time. Perform other assigned tasks. What we're looking for : Scientific degree. At least 1 year of experience in CRO, biotech, pharma, or research institutes in a similar role (preferred). Knowledge of HA requirements related to pharmaceutical research and SAS programming. Knowledge in statistics and its applications to clinical trials. Proficiency in SAS and CDISC standards (SDTM, ADaM). Fluent in English. Planning and organizational skills. Strong communication skills. Team-oriented mindset. What we offer : Competitive salary, bonuses, and benefits, along with opportunities for professional development within an expanding international company. Please review the personal data processing notice on our website. Who we are : OPIS is an international CRO with 25 years of experience in conducting various clinical studies globally. We provide state-of-the-art technology and innovative solutions across all phases of drug trials, including medical devices. Our global locations enable us to offer comprehensive clinical research services, including scientific advice, medical writing, trial management, data management, statistics, pharmacovigilance, and quality assurance. J-18808-Ljbffr

Location: puglia, IT

Posted Date: 5/9/2025