Date:         Mon, 5 May 1997 15:38:38 GMT
Reply-To:     Michael Wulfsohn <mwulfsohn@WORLDNET.ATT.NET>
Sender:       "SAS(r) Discussion" <SAS-L@UGA.CC.UGA.EDU>
From:         Michael Wulfsohn <mwulfsohn@WORLDNET.ATT.NET>
Organization: Gilead Sciences
Subject:      Biostatistics positions at Gilead Sciences

                Medicine At The Core Of Life
 
Few biotechnology companies can offer you the promise and excitement of
Gilead Sciences.  We are a leader in the discovery and development of a
new class of broad spectrum antiviral therapeutics that may provide
powerful new treatments for CMV retinitis, HIV, influenza and other
viruses.  Here, you'll be a part of a company that takes pride in its
achievements, knowing that patients may benefit from the products we
create.  Come join us in any of the following opportunities and
contribute to our Biometrics group.
 
Manager, Biometrics
-------------------
Acting as a team leader for a group of statistical programmers involved
in NDA submissions, you will provide input on automating statistical
reporting, design statistical analyses, and write up methodology and
results sections of study reports. You will need a PhD and 5 years
pharmaceutical experience. Applied statistical knowledge, experience
with NDA submissions, excellent oral/written communication abilities,
SAS programming skills (including macros), and knowledge of database
design are required.
 
Statistical Analysts
--------------------
Responsible for performing statistical analyses of clinical trial data,
and writing analysis plans, results sections of clinical reports.
You will also be involved in implementing an efficient programming
infrastructure for automated tracking and reporting for clinical
trials.  This will include creating a library of SAS macros and
resalable tools and maintaining a seamless interface between Clintrials,
wordprocessors and SAS and connectivity for remote SAS users.  You will
also create a GUI report interface for clinical and data management
users and provide users the ability to browse CRFs, data listings and
summaries.  Along with a Masters in Statistics and 5 years relevant
experience, we require strong skills in these areas: SAS macros; SAS-AF;
SAS-EIS; SAS-Graph; SAS-FSP; structured programming; UNIX.  Excellent
analytical, writing and communication skills are also essential.
 
Statistical Programmer
----------------------
You will perform analyses of clinical trial data, including listings,
tabulations, graphical summaries and formal statistical estimates and
tests.  You will also edit specifications for quality control of data,
perform cross study analyses and use SAS macros to automate all of the
above functions.  We will also rely on you to develop reporting analysis
plans for new studies and assist in the preparation of NDAs.  Your
Master's degree in Statistics should be supported by 3 years of
experience demonstating skill in the following areas:  SAS-Stat,
SAS-Graph, SAS macros, structured programming, and statistical
analysis.  Good oral and written communication abilities and analytical
skills are required.
 
At Gilead, we are committed to developing important treatments for a
wide range of viral diseases, from influenza to AIDS.  As you will
discover, we are as committed to opportunity as we are to scientific
achievement.  Interested candidates should send a resume, indicating
position of interest, to: Human Resources, Gilead Sciences, Inc., 333
Lakeside Drive, Foster City, CA  94404, fax (415) 573-4800. Or check our
website: www.gilead.com. We are proud to be an equal opportunity employer.
 
GILEAD SCIENCES