Sr SAS Programmer
Can be remote but prefers RTP NC Market or East Coast (EST)
Our Client seeking Sr Programmer dedicated to a program that will have a BLA submission 4Q27.
High-level needs are review of SDTM / ADaM datasets, eCRT packages, ad-hoc requests and programmatically supporting data management.
The Contract Statistical Programmer is responsible for:
creating programs to develop, validate, and document datasets, tables, listings, and figures related to the compounds being studied.
The focus for this position will be on support of clinical development and post-marketing activities.
Sr Programming expertise is needed for data review and to support scientific publications and other requests for medical affairs.
SKILLS/DUTIES
The Contract Statistical Programmer must have experience in the use of SAS software for analysis of clinical trial data and knowledge of
CDISC standards.
A list of essential duties and responsibilities are listed as follows:
• Function as support programmer for one or more compounds under study.
• Provides SAS programming of tables, listings, figures to support the needs of internal monitoring and analysis, including graphical displays for scientific publications as needed.
• Supports programming for clinical study reports, as needed, including support of statistical programming for outsourced trials.
• In collaboration with data management, may provide specialty SAS programming for data management including customized line listings to support review of clinical trial data.
• Ensures that study documentation is maintained to the standard required according to SOPs and acceptable for audit.
• Ability to communicate technical concepts to others.
• All other duties as assigned.