Senior Statistical Programmer 1
KochiFull-time4–7 yrsPosted 6 days ago
Mid-level pharma role at Worldwide in Kochi. Needs 4+ years.
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
- SAS
- Clinical research
- SQL
- Clinical data management
- Documentation
- SOP writing
Good to have
- VBA
- Data privacy