REQUIREMENTS

Masters or PhD in Statistics
5+ years experience
3-5 years Pharma experience

DESCRIPTION

Provide guidance on statistical analyses, tabulations, graphics and listings of clinical trial data (Phase II and III). Offer recommendations in statistical analysis methodology. Ability to coordinate with SAS Programming in the production of data displays. Provides statistical analyses in the support of product development, including New Drug applications (NDA's) and Biological License Applications (BLA's) submissions. Ensure integrated summaries (ISS and ISE) for clinical/statistical submissions, guaranteeing that the submissions meet regulatory and company standards.

OTHER DETAILS

Salary commensurate with experience
Health/Dental/Retirement Plans Offered
This starts as a 6 month contract positions and may be extended or made into a full time permanent position. Major pharmaceutical company is the client.

Send your resume and salary requirements to resumes[at]informationpros.com

[Please reference Bioinformatics.Org when responding to this announcement.]