Senior SAS Developer (SDTM)
PSI CRO
$0-$0 / yr
Salary
brazil
Region
ASAP
Start Date
About PSI CRO
PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
About this Role.
We 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:
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
Sufficient relevant technical experience
Experience in Clinical Data Management systems (like Medidata/Veeva) is desirable
Knowledge of and experience in the SAS programming language (Base SAS, SAS/Macros, SAS/ODS)
Knowledge of CDISC standards
Knowledge of and experience in SQL
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.