Will provide quality statistical programming support for clinical trials conducted for regulatory submission to government agencies. Will work with and assist statisticians in the summary of clinical trial data for clinical trial reports, including summary tables, data listings, and figures. Familiarity with statistical analysis is essential.

M.S. in Statistics or Biostatistics with 2 to 5 years of industrial clinical trial experience. Good verbal and written communication skills, good interpersonal skills and proficiency with statistical software, particularly SAS are required.

Please forward resume with salary/rate requirements to: Scott --> scott@marshwinds.net