Dear Assocaites,

REQ:SAS Developer


DUTIES AND RESPONSIBILITIES



DUTIES >>   ***Strong possibility of extension through at least June 2009.

Provide statistical analyses, tabulations, graphics and listings of clinical
trial data. Offer guidance in statistical analysis methodology.  Ability to
coordinate the production of data displays in an efficient manner for
inclusion in integrated clinical/statistical reports and and other similar
reports.  Provides statistical analyses, summaries and reports of studies in
the support of product development including New Drug applications

(NDA's) and Biological License Applications (BLA's) submissions.

Ensuring statistical and integrated clinical/statistical reports meet
regulatory and company standards.  Presents and interprets data
manipulations/processing and statistical analyses.  Derives statistical
conclusions and makes recommendations based on experimental results.



SKILLS >>   Broad understanding of statistical methods within context of
skills and ability to communicate effectively. Ability to complete tasks
under limited supervision. A minimum of two years of pharma and/or biotech
experience preferred.



EDUCATION >>   MS or Ph.D. degree in Biostatistics or related field.

clinical trials. Broad knowledge of SAS and UNIX. Proven ability to organize
workload and priorities and complete tasks on time. Demonstrated ability to
work effectively in a team environment. Strong interperson



*Thanks & Regards***

*Jenson
Technical Recruiter
Sedna Consulting Group
Phone: 609 632 0201
Fax     : 609-228-4366
Email: [EMAIL PROTECTED]
**Website: **www.sednacg.com <http://www.sednacg.com+/>*

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