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, or 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 validation documents. Liaise with Data Management team and develop SAS programs/macros/utilities to detect data discrepancies. Develop SAS programs to import/reconcile external clinical data. Develop and validate SAS programs for identifying Non-Protocol Deviations. Collaborate with Biostatistics and Data Management staff on clinical trials/projects. Maintain and archive SAS programming documentation. Assist in establishing and maintaining SOPs and templates related to Statistical SAS programming. Stay informed on new SAS developments relevant to clinical trial data management. Ensure KPI and metrics are met for assigned studies. Complete required trainings on time. Complete daily entries in the TRACK system accurately. Perform other assigned tasks. What we're looking for : At least 1 year of experience in CRO, biotech, pharma, or research institutes in a similar role is preferred. Knowledge of HA requirements related to pharmaceutical research and SAS programming. Knowledge of statistics and its applications to clinical trials. Proficiency in SAS and CDISC standards (SDTM, ADaM). Planning and organizational skills. Team-oriented attitude. What we offer : We offer a competitive salary, bonuses, and benefits, along with opportunities for professional development within an expanding international company. Please read the data processing notice on our website. Who we are : OPIS is an international CRO with 25 years of experience in conducting various clinical studies worldwide. We provide innovative IT solutions and comprehensive services across all phases of drug trials, including medical devices. Our global locations support a full spectrum of clinical research services. J-18808-Ljbffr

Location: Vicenza, Veneto, IT

Posted Date: 7/4/2025