Date:         Fri, 19 Sep 2008 14:23:29 -0400
Reply-To:     Randi Schoenfelder <rschoenfelder@THEODOLITEHC.COM>
Sender:       "SAS(r) Discussion" <SAS-L@LISTSERV.UGA.EDU>
From:         Randi Schoenfelder <rschoenfelder@THEODOLITEHC.COM>
Subject:      Positions Available

Hello Everyone,
Due to growth, our client has several positions available at various
levels for strong biostatisticians. The company is a leading solutions-
driven company that provides expertise to biopharmaceutical and medical
device companies. This is a few of the positions they have available for
strong biostatisticians. Their goal is to hire and retain highly dynamic
and talented professionals. Currently they are searching for innovative
thinkers looking to make a difference in their professional and personal
career goals.

More detailed information can be provided to potential candidates.
Interested candidates can forward a confidential CV to
rschoenfelder@theodolitehc.com.  You may also contact Randi Schoenfelder
via phone at 732-625-1708.

Locations: Various US locations depending on position:
(San Diego CA, Marietta GA, Bloomingdale IL, Austin TX)


DIRECTOR OF BIOSTATISTICS Serves as core team member for larger projects.
Working in a supervisory capacity, coaches the technical evolution of the
work product and reviews client deliverables for compliance with project
specifications. Minimum seven years experience (or five years plus Ph.D.)
in pharmaceutical development and working knowledge of SAS for statistical
analysis

ASSOCIATE DIRECTOR BIOSTATISTICS - Serves as core team member for larger
projects. Working in a supervisory capacity, coaches the technical
evolution of the work product and reviews client deliverables for
compliance with project specifications. Minimum seven years experience (or
five years plus Ph.D.) in pharmaceutical development and working knowledge
of SAS for statistical analysis

MANAGER/SR. MANAGER OR ASSOCIATE DIRECTOR OF CLINICAL PROGRAMMING -
(Title will vary depending on experience) Responsible for the successful
operation of the Biometrics Technical Operations programming teams.
Ultimate responsibility for all projects in the area of technical support
to Biometrics, primarily Data Operations but also working to improve
quality and efficiency with which deliverables and initiatives are
completed.

SR. BIOSTATISTICIAN II Capably applies knowledge of statistics to
independently generate tables, listings, and graphs of clinical trial data
using SAS. Performs quality control of TLGs and derived data sets created
by other statisticians and may be asked to assist in the preparation of
statistical plans.

SR. BIOSTATISTICIAN I Capably applies knowledge of statistics to
independently generate tables, listings, and graphs of clinical trial data
using SAS. Interacts with clients on statistical issues, provides guidance
to other employees on technical issues, prepares complex (non-
conventional) draft statistical plans and reports, and is able to QA/QC
TLGs and derived data sets created by other statisticians.
Thanks so much!
Randi