Communication point for data management and statistics on matters of database programming and deliverable database development
Clinical database (EDC) requirements/structure review and testing
Data validation plan review and programming of data validation procedures
Generation of clinical database listings and reports to support clinical trial data collection, tracking, review and validation
Programming of patient profiles
Participate and support the development of Study Data Tabulation Model (SDTM) (define.xml, annotated CRF, reviewer’s guide) and programming of data transformation from raw data sources into CDISC-complaint deliverable
Validation of clinical trial data according to SDTM specifications
Deliverable database transfer to clients; electronic data transfers
Liaison with vendors and clients regarding electronic data transfer specifications
Receipt and validation of electronic data transfers

College or University degree (IT, programming, technical education)
Full working proficiency in English
At least two years of industry experience
Knowledge of and experience in the SAS programming language (Base SAS, SAS/Macros, SAS/ODS) is required
Knowledge of and experience in SQL
Experience in Clinical Data Management systems (like Medidata/Veeva) is desirable
Knowledge of CDISC standards is a plus
Proficient user of standard MS Office applications and MS Access
Experience in a professional environment, preferably with clinical or medical data
Only CVs in English will be considered.

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SAS Developer, SDTM

Key skills