Requirements: English
Company: JR Italy
Region: Como , Lombardia
Job Title: Junior Statistical SAS ProgrammerThe Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is primarily responsible for developing SAS programs to generate datasets, tables, figures, and listings for clinical studies, publications, or Health Authorities requests. This role involves collaboration with Biostatistics and Data Management teams on clinical trials and projects.Key Responsibilities:Develop SAS programs for datasets, tables, figures, and listings in line with ICH E3 guidelines, publications, and Health Authorities requests.Utilize CDISC standards to generate SDTM and ADaM datasets.Write programming specifications for analysis datasets.Validate ADaM datasets using Pinnacle 21.Maintain and archive CDISC documentation, including Define.xml and ADRG files.Contribute to the development of standard SAS macros and validation documents.Coordinate with Data Management to develop programs and macros for data discrepancy detection.Handle external clinical data, developing programs for data import and reconciliation.Develop and validate SAS programs for identifying Non-Protocol Deviations.Collaborate with Biostatistics and Data Management teams on clinical projects.Maintain SAS programming documentation.Assist in establishing and maintaining SOPs and related templates for statistical SAS programming.Stay informed on new SAS developments relevant to clinical data management and update the team accordingly.Ensure KPI and metrics for studies are achieved.Complete required trainings on time, including study-specific, OPIS, and Sponsor SOPs.Accurately update the daily TRACK system with billable and non-billable hours.Perform additional tasks as assigned.Qualifications:Minimum of 1 year 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.Understanding of statistics and its application in clinical trials.Proficiency in SAS and CDISC standards (SDTM, ADaM).Strong planning and organizational skills.Team-oriented mindset.What We Offer:Competitive salary, bonuses, and benefits, along with opportunities for professional growth within an expanding international company.Please review the personal data processing notice available on our company website.About Us:OPIS is an international CRO with 25 years of experience in conducting Phase I-IV, non-interventional, and medical device studies globally. We leverage advanced technology and innovative approaches to manage complex projects across various therapeutic areas, providing comprehensive clinical research services worldwide.#J-18808-Ljbffr