Technogen International Company
Sr. SAS Programmer
Technogen International Company, Pasadena, CA
Please Note: As of July 22, 2021, our team will require that all candidate submissions include a LinkedIn profile. Please do not submit any candidates that do not have a LinkedIn.
Provide statistical programming for regulatory submissions and publications, and ad hoc or post hoc analyses. Generate analysis data sets, listings, tables and figures, as well as supporting documentation. Function as lead programmer on single or multi-protocol projects, and participate in project team meetings. Assume protocol level responsibilities in statistical programming. Review protocol and SAP, write/review analysis data specifications, etc. Interact with Statisticians, Clinical Data Programmers, Data Managers, Clinical Operations personnel and project manager to ensure the timeline and quality of analysis data and reporting. Independently validate SAS data sets and outputs from CROs or other programmers. Prepare validation documentation. Develop and maintain SAS programming infrastructure, macros and standards. Adhere to the company s and departmental SOPs, Working Instructions and Standards. Participate in the company s development and implementation of global analysis data standards, output formats, standard SAS programs, etc.
JOB CLOSED!
Required Skills : Bachelor s Degree preferred or equivalent years of experience Years of Experience: 5 Years of Experience with Software development and SQL
Basic Qualification :
Additional Skills :
Rank :C1
Requested Date :2023-01-20
Provide statistical programming for regulatory submissions and publications, and ad hoc or post hoc analyses. Generate analysis data sets, listings, tables and figures, as well as supporting documentation. Function as lead programmer on single or multi-protocol projects, and participate in project team meetings. Assume protocol level responsibilities in statistical programming. Review protocol and SAP, write/review analysis data specifications, etc. Interact with Statisticians, Clinical Data Programmers, Data Managers, Clinical Operations personnel and project manager to ensure the timeline and quality of analysis data and reporting. Independently validate SAS data sets and outputs from CROs or other programmers. Prepare validation documentation. Develop and maintain SAS programming infrastructure, macros and standards. Adhere to the company s and departmental SOPs, Working Instructions and Standards. Participate in the company s development and implementation of global analysis data standards, output formats, standard SAS programs, etc.
JOB CLOSED!
Required Skills : Bachelor s Degree preferred or equivalent years of experience Years of Experience: 5 Years of Experience with Software development and SQL
Basic Qualification :
Additional Skills :
Rank :C1
Requested Date :2023-01-20