Senior Statistical Programmer (12-171) FibroGen
As a member of a clinical project team, this individual will perform the following key tasks:
Participate in CRF design, database review, data management plan, data review, data validation procedures, and review of data listings.
Design, develop, implement, and maintain software for the monitoring of ongoing studies, reporting, and analysis of clinical trials.
Provide consistency across protocols within a project on CRFs, database design, analysis files, and tables, listings, and graphs.
Produce data listings, summary tables and graphics for interim and final analyses and publications.
Create statistical files for statistical analysis. Integrate data across studies within a project. Test, document, review and validate all programs according to department guidelines.
Provide consulting and systems support for applications software. Develop new applications software and identify key feature set.
Coordinate data transfer and/or programming standards with CROs and vendors. Work with minimal supervision.
MA/MS in a related field with 5 years experience, or BA/BS in computer science, statistics, math with 7 years experience.
Minimum of 7 years of SAS programming and 5 years of clinical trial experience.
Expertise in SAS programming language (especially data step, and summarization procedures), report generation, and standards for programming and validation.
Experienced in macro writing. Knowledge of advanced statistical procedures in SAS including LIFETEST, MIXED, GLM, especially SAS/GRAPH.
Experience with CDISC data standards required.
Knowledge of database and data warehouse theory. Data mining experience is a plus.
Understanding of regulatory guidelines that affect statistical deliverable.
Ability to work on multiple tasks simultaneously and meet project deadlines.
Good verbal and written communication skills.
Mandarin language skills is a plus
||San Francisco, CA |