Biostatistician Req # 433535
Malvern PA
- Perform statistical activities supporting clinical trial, e.g. randomization/data review, interaction with study manager and data manager.
- Write in conjunction with the clinical trial team the statistical analysis plan (SAP) and the table shell document.
- Perform statistical analyses as defined in SAP or as requested such as graphical displays of results, sensitivity analyses, outlier detection, and evaluation of model fit.
- Perform and document quality control of tables, listings, and graphs (TLG), as defined in the SAP.
- Review and quality control derived variables for analysis data sets.
- Develop and document data/programming specifications jointly with programmers.
- Review clinical study report (CSR).
- The candidate should have solid statistical and SAS programming skills.
- Candidate should have at least 2-years pharmaceutical industry experience and a previous experience in oncology.
- MS or PhD in Biostatistics or Statistics.
Please let me know if you are interested and the best way/time to reach you for a full discussion.
Douglas Beman
Corporate Recruiter
Ph: (732)-675-9465
Email: doug@iconma.com
Web Site: www.iconma.com
http://www.linkedin.com/pub/douglas-j-beman/2/952/265
Last updated: 8/25/2010