Requirements: English
Company: PSI CRO AG
Region: Milan , Lombardy
6 days ago Be among the first 25 applicantsCompany DescriptionWe are the company that cares for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.Job DescriptionWe are currently looking for a knowledgeable and proactive SAS Developer to join our global Data Management team.Please note the official PSI CRO job title will be: Senior Database Developer. If you are keen to provide the full range of clinical database development and programming services, ensure high quality, accuracy, and consistency of clinical data, and be involved in something new, outstanding and challenging, this job opportunity is perfect for you!Responsibilities:Serve as a communication point for data management and statistics on database programming and deliverables.Review and test clinical database (EDC) requirements and structure.Review data validation plans and program data validation procedures.Generate clinical database listings and reports to support data collection, tracking, review, and validation in clinical trials.Program patient profiles.Participate in developing Study Data Tabulation Model (SDTM) including define.xml, annotated CRF, reviewers guide, and program data transformation into CDISC-compliant formats.Validate clinical trial data according to SDTM standards.Transfer deliverable databases to clients electronically.Liaise with vendors and clients regarding electronic data transfer specifications.Validate electronic data transfers received.Qualifications:College or University degree in IT, programming, or technical field.Full professional proficiency in English.Relevant technical experience in clinical data management or related fields.Experience with Clinical Data Management systems (e.g., Medidata, Veeva) is desirable.Proficiency in SAS programming (Base SAS, SAS/Macros, SAS/ODS).Knowledge of CDISC standards.Experience with SQL.Proficient in MS Office applications and MS Access.Experience working with clinical or medical data in a professional environment.Additional Information:If you wish to showcase your skills and knowledge within a growing company that values its people, this is the right opportunity for you.Seniority levelMid-Senior levelEmployment typeFull-timeJob functionInformation TechnologyIndustriesPharmaceutical Manufacturing#J-18808-Ljbffr