PThe 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. /ppbSome of what you'll do : /b /pulliDevelop SAS programs for generating datasets, tables, figures, and listings for clinical trials (according to ICH E3), publications, or Health Authorities requests /liliUse CDISC guidelines to generate SDTM / ADaM datasets /liliWrite Programming Specifications for analysis datasets /liliValidate ADaM datasets using Pinnacle 21 /liliPrepare, maintain, and archive CDISC documentation for ADaM (Define.xml and ADRG) /liliContribute to developing standard SAS macros and prepare validation documents /liliLiaise with Data Management team to develop SAS programs/macros/utilities to detect data discrepancies /liliHandle external clinical data and develop SAS programs to import/reconcile it /liliDevelop and validate SAS programs for identifying Non-Protocol Deviations /liliCollaborate with Biostatistics and Data Management staff on clinical trials/projects /liliMaintain and archive SAS programming documentation /liliEstablish and maintain SOPs, forms, and templates related to Statistical SAS programming /liliMaintain document/programming standards /liliStay informed on new SAS developments relevant to clinical trial data management and update the Direct Manager /liliEnsure KPI and metrics for assigned studies are met /liliComplete required trainings on time /liliAccurately complete daily entries in the TRACK system /liliPerform other tasks as assigned /li /ulpbWhat we're looking for : /b /pulliAt least 1 year of experience in CRO, biotech, pharma, or research institutes in a similar role (preferred) /liliKnowledge of HA requirements related to pharmaceutical research and SAS programming /liliKnowledge of statistics and its applications to clinical trials /liliKnowledge of SAS and CDISC standards (SDTM, ADaM) /liliStrong planning and organizational skills /liliTeam-oriented attitude /li /ulpbWhat we offer : /b /ppWe offer a competitive salary, bonuses, and benefits, along with opportunities for professional development within an expanding international company. /ppPlease review the personal data processing notice on our company website. /ppbWho we are : /b /ppOPIS is an international CRO with 25 years of experience in conducting Phase I-IV, non-interventional, and medical device studies worldwide. We provide state-of-the-art IT solutions and innovative approaches to complex projects. /ppOur expertise covers all phases of drug-related trials, supporting sponsors beyond therapeutic areas, and offering clinical investigations for medical and diagnostic devices. With global locations, we provide comprehensive clinical research services including scientific advice, medical writing, trial start-up, monitoring, study management, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture, quality assurance, and training. /p #J-18808-Ljbffr