Vacancy expired!
- Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for SDTM datasets.
- Following statistical analysis plans and the Analysis Data Model (ADaM) Implementation Guide, writes specifications for analysis datasets.
- Following specifications, develops algorithms and writes programs to create datasets.
- Produces data listings, summary tables and graphs using SAS software.
- Independently checks data listings, summary tables and graphs.
- Imports and exports SAS data.
- Assists data management group in performing data edit checks.
- Understands and conducts work consistent with Google Cloud Platform, ICH, 21 CFR part 11, internal SOPs and training, and international regulatory requirements.
- Plays an active role in taking project solutions and generalizing them for the Biostatistics group.
- Interacts with the project statistician and guides other programmers participating on a project team.
- Bachelor's degree in a statistic, computer science, or a similar quantitative field; an equivalent combination of relevant education and applicable job experience may be considered.
- Experience in programming with the Statistical Analysis System (SAS) beyond classroom work is required.
- Minimum of 5 years' experience in clinical statistical programming within pharmaceutical or related industry (biotechnology, medical device, Clinical Research Organization (CRO).
- SAS Certified Base and/or Advance Programmer experience is preferred.
- Proven experience in SAS programming including base SAS, SAS/Stat, SAS/Graph, macros, ODS.
- Experience with SDTM and ADaM industry data standards.
- Exposure to statistical graphics software.
- Able to assert own ideas and persuade others through effectively consolidating, evaluating, and presenting relevant information.
Vacancy expired!