Associate Clinical SAS Programmer
Tasks
- Annotate and update CRF annotations for post production changes
- Assemble database components layouts derivations validations edit checks
- Build non standard objects from scratch
- Collaborate with R and D functions
- Configure Coder module
- Coordinate internal and external resources for R and D deliverables
- Copy create and customize study database objects from global library
- Create and maintain global library user guide
- Define scope and conduct impact analysis for migrations and changes
- Deploy, validate, test, and implement electronic data capture systems
- Design, develop, and maintain clinical databases
- Ensure data integrity data quality validation compliance
- Generate annotated and non-annotated case report forms
- Maintain case report forms database objects edit checks and procedures
- Migrate databases
- Participate in UAT for new application releases
- Perform quality assurance on DBD internal audit process
- Perform self testing for database objects
- Support clinical data management processes
- Troubleshoot and maintain data management tools and documentation
Perks/Benefits
- N/A
Skills/Tech-stack
Case Report Form | Clinical Database | DBD | Data Capture | Edit checks | Electronic Data | Electronic data capture | GxP | Master File | SAS | SAS programming | Trial Master | Trial Master File | UAT
Education
N/A
Roles
Clinical Data Manager | Data Manager | Manager | Programmer | SAS Programmer
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