Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.Job DescriptionROLEThe Database Programmer contributes to develop the clinical database to collect the clinical data provided on paper or electronic CRFs, program the computerized checks or SAS checks and ensures clean, accurate and complete clinical data can be delivered to customers at the highest quality in accordance with the project plan and study timelines.KEY RESPONSABILITIESCreate the annotated CRF (aCRF) using company standards or sponsor’s naming conventions in accordance to relevant company proceduresBuild the clinical database, creating variables, codelists, forms and visits in accordance with the aCRFDevelop the computerized checks in accordance with the Data Validation PlanDevelop SAS checks in accordance with the Data Validation PlanValidate the database structure and the computerized checks or SAS checksImplement mid study changes to the production eCRFCreate and validate import programs of electronic data received from external vendorsImport electronic data received from external vendorsProgram and validate data listings (e.g. Manual checks, Medical Review listings, Coding report etc)Program and validate tracking or metric reportsPlan and prioritise his/her own work and take appropriate actions (e.g., escalation)Apply SOPs and guidance documents as well as applicable industry standards like ICH, GCP etc to day-to-day activities generating all the required documentation for study filesMonitor progress of activities and communicate the status of activities and the achievement of milestones to the Lead DMMaintain continuous and appropriate communication with Lead DM and share critical and general issuesConduct other activities as requiredDESIRED QUALIFICATION & EXPERIENCEDegree (preferably in Computer Science) or at least 1 year of experience in database programming or similar field in a pharmaceutical environment or equivalentKnowledge of Alira Health systems, FairBasic understanding of pharmaceutical industry guidelines like ICH, GCP etcBasic understanding of Data Management processesTECHNICAL COMPETENCES & SOFT SKILLSKnowledge of SAS programming, FairEnglish, FairMS Office Suite, GoodProfessionalTrustworthyAbility to effectively prioritizeQuality focusedPersonable AttitudeWillingness to learnTeam PlayerContract Type Intern (Fixed Term) (Trainee)