Redbock - an NES Fircroft company
Sr. Statistical Programmer
Redbock - an NES Fircroft company, Fremont, California, United States
***W2 ONLY***
PLEASE NO THIRD PARTIES
SUMMARY: A thriving Bay area biotech company is looking for an experienced Senior Statistical Programmer to support their team. This is an exciting, long-term opportunity with a leading company in one of the major pharma/biotech hubs in the country. This role is fully remote. This consultant must have strong CDISC knowledge (proficiency in SDTM and ADaM programming), strong TLG skills, and must be comfortable interpreting specifications.
DUTIES & RESPONSIBILITIES: Perform data manipulation, analysis and reporting of primarily clinical trial data Create analysis data sets (ADaM & SDTM) Program and generate tables, listings and graphs (TLGs) Validate and document SAS programs and output Fulfill ad-hoc analysis requests Other services as needed
QUALIFICATIONS & REQUIREMENTS: Bachelor’s degree or equivalent and a minimum of 12+ years’ of SAS programming experience in the pharmaceutical/biotech industry Strong CDISC experience – SDTM & ADaM Experience interpreting specifications Experience creating source and validation programs using SAS software for ADaM & SDTM datasets, analysis datasets, and tables, listings, and graphs (TLGs) for multiple studies/products; Experience integrating data across multiple studies or drug programs; Expertise in the development and use of system-level macro programs;
LOCATION: Work will be performed remotely. Core PST hours.
PLEASE NO THIRD PARTIES
SUMMARY: A thriving Bay area biotech company is looking for an experienced Senior Statistical Programmer to support their team. This is an exciting, long-term opportunity with a leading company in one of the major pharma/biotech hubs in the country. This role is fully remote. This consultant must have strong CDISC knowledge (proficiency in SDTM and ADaM programming), strong TLG skills, and must be comfortable interpreting specifications.
DUTIES & RESPONSIBILITIES: Perform data manipulation, analysis and reporting of primarily clinical trial data Create analysis data sets (ADaM & SDTM) Program and generate tables, listings and graphs (TLGs) Validate and document SAS programs and output Fulfill ad-hoc analysis requests Other services as needed
QUALIFICATIONS & REQUIREMENTS: Bachelor’s degree or equivalent and a minimum of 12+ years’ of SAS programming experience in the pharmaceutical/biotech industry Strong CDISC experience – SDTM & ADaM Experience interpreting specifications Experience creating source and validation programs using SAS software for ADaM & SDTM datasets, analysis datasets, and tables, listings, and graphs (TLGs) for multiple studies/products; Experience integrating data across multiple studies or drug programs; Expertise in the development and use of system-level macro programs;
LOCATION: Work will be performed remotely. Core PST hours.