Description
Lead Statistical ProgrammerA leading Biopharmaceutical company in San Francisco is entering Phase II trials for one of their compounds and is looking to bring a Lead Statistical Programmer on board. Among others, this client specializes in CNS, Immunology and Oncology. This is an onsite, full-time position.
The following provides a more detailed description of day to day duties:
- Provides critical clinical programming support to projects.
- Interacts directly and independently with Biostatisticians, Data Management, Programmers, Clinical Development staff and management as a fully functioning member of the clinical programming team.
- Proactively keeps the manager updated on the status, programming accomplishments and criticality of any issues impacting the quality and timely delivery of SAS Programming outputs.
- Actively solicits feedback from manager to address any issues and/or complex problems
- Leads in the development of analysis data set specifications.
- Independently implements and champions the use of standards and TA specific data listings, summary tables, and figures as specified in statistical analysis plan in the clinical study report.
- Develops robust, flexible SAS macro programs or modules that generate standard outputs and/or facilitate CDISC implementation.
- Ensures compliance of standards for all SAS programming assignments.
- Reviews and provides feedback on eCRF designs, eCRF annotations, DB structures, edit checks, SAPs and SPPs.
Position Requirements:
- MS/MA in Statistics or other relevant field
- 6+ years pharmaceutical industry experience
If interested in this position or looking for more information, please respond to this posting.
To find out more about Real please visit www.realstaffing.com