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 for 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 to develop SAS programs/macros/utilities for discrepancy detection. Handle external clinical data requirements and develop SAS programs to import/reconcile such 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. Establish and maintain SOPs, templates, and standards related to SAS programming. Stay informed on new SAS developments relevant to clinical trial data management. Ensure KPIs and metrics are met for assigned studies. Complete required trainings on time. Perform daily entries in the TRACK system accurately. 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 of statistics and their applications to clinical trials. Proficiency in SAS and CDISC standards (SDTM, ADaM). Fluency in English. Planning and organizational skills. Good communication skills. Team-oriented mindset. What we offer : Competitive salary, bonuses, and benefits, along with career development opportunities in an expanding international company. Please review the personal data processing notice on our website. Who we are : OPIS is a 25-year-old international CRO conducting Phase I-IV, non-interventional, and medical device studies globally. We provide state-of-the-art IT solutions and innovative approaches to complex projects, covering all phases of drug trials and medical device investigations, with locations worldwide offering comprehensive clinical research services. J-18808-Ljbffr

Location: campania, IT

Posted Date: 6/7/2025