Senior Statistical Programmer 1

About the role

Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research. *SUMMARY: To perform the lead programming role, lead continuous improvement in the programming function's operating systems and provide consultancy across the function*

What you'll do

• _Some team members may focus on a limited number of these responsibilities depending on requirements. __Tasks may include but are not limited to:_
• Develop, test and execute SAS programs to produce and validate CDISC SDTM and ADaM datasets, tables, figures and listings (TFL)
• Perform review and provide guidance on the development of the clinical database specification, data transfer agreement/specification, specification of tables
• Develop and review specification for SDTM datasets and ADaM datasets for safety data, TFL shells and other specifications, e.g. patient profiles, OPS reports
• Develop and review electronic data submission package (SDTM annotated CRF, define.xml, Study/Analysis Data Reviewer's Guide) for high complexity studies

What you need

• 4–7 yrs of experience
• SAS
• Clinical research
• SQL
• Clinical data management
• Documentation
• SOP writing
• Any graduate

Good to have

• VBA
• Data privacy