[IEEE-bhpjobs] [Fwd: JobWatch E-mail Notification]

[Esther L.]

-------- Original Message --------
Subject: JobWatch E-mail Notification
Date: Mon, 15 Aug 2005 14:44:39 (GMT)
From: JobWatch <jns at centerwatch.com>
Reply-To: cw.jobwatch at thomson.com
To: esther-l at mailsnare.net <esther-l at mailsnare.net>

Dear Clinical Research Professional:

Post Your Resume!!! Join over 500 of your colleagues in Clinical 
Research who
have already posted their resumes and are now receiving calls from 
employers.
The JobWatch Resume Database Service provides employers specializing in
clinical research with easy access to your resume--at no cost to you. When
you create an account and place your resume in the JobWatch database you may
keep your contact information confidential, fully protecting your privacy
while allowing employers to contact you via e-mail sent through CenterWatch.

Why not increase your exposure to employers and give this service a try?
Visit http://www.centerwatch.com/careers/resdat/seeker/ now!


JobWatch is pleased to inform you of the following new opportunities in the
clinical research industry (in the specific categories you requested):

Positions in: Data Management

   Advanced Associate External Data Manager, MedFocus Consulting
Opportunities, Wallingford, CT
   Clinical Data Specialist (Clinical Data Management) mid-senior level, 
Duke
Clinical Research Institute (DCRI), Durham, NC
   Clinical Data Analysts (All Levels), PPD Development, Texas and North
Carolina, XX
   Manager, Clinical Data Management, PPD Development, All Locations, XX
   Associate Director, Clinical Data Management, PPD Development, North
Carolina and Texas, XX
   Sr. Clinical Data Analyst (Technical Operations), PPD Development, North
Carolina and Texas, XX
   Clinical Data Associate (Chicago, IL, Thousand Oaks, CA, and Old 
Lyme, CT,
Cincinnati, OH), Kendle International, Inc, All Locations, XX
   Manager, Clinical Data Operations (Chicago, IL), Kendle 
International, Inc,
Chicago, IL
   Clinical Data Manager (Thousand Oaks, CA, Cincinnati, OH, and 
Chicago, IL),
Kendle International, Inc, Cincinnati, OH
   Document Specialist III, SAIC- Frederick, Inc, Frederick, MD
   Data Manager, aaiPharma, Natick, MA
   Clinical Data Coordinator, aaiPharma, Natick, MA
   Clinical Data Management Lead, aaiPharma, Mississauga, XX
   Clinical Data Manager, Bristol-Myers Squibb, Wallingford, CT
   Analyst, Bristol-Myers Squibb, Wallingford, CT
   Nurse Manager, Office of Clinical Research, Tulane Cancer Center, New
Orleans, LA
   Director of Clinical Data Management, Abeo Resources, Northeast, XX
   Clinical Data Manager, Metropolitan Research Associates (MRA), Boston, MA


Positions in: Information Systems

   Associate  SR and Jr Clinical SAS Programmers-Entire Team Needed, 
MedFocus
Consulting Opportunities, Philadelphia, PA
   Programmer Analyst/Sr. Programmer Analyst, PPD Development, All 
Locations,
XX
   Manager, SAS Programming, PPD Development, All Locations, XX
   Associate Director/Director of SAS Programming, PPD Development, 
Hamilton,
NJ
   Director, IT, Essential Group, Inc., Gurnee, IL


Positions in: Regulatory Affairs

   Safety Associate, MedFocus Consulting Opportunities, Central, NJ
   Senior Quality Assurance Auditor, Paragon Biomedical, Inc, Irvine, CA
   Contract Regulatory Associate, MedFocus Consulting Opportunities,
Indianapolis, IN
   Pharmacokineticist, West Coast Clinical Trials, Costa Mesa, CA
   Senior Auditor, Bristol-Myers Squibb, Wallingford, CT
   Director of Research, University Hospital, Louisville, KY
   Senior Regulatory Affairs Specialist, Medtronic Vascular, Santa Rosa, CA
   Regulatory Affairs Manager, Medtronic Vascular, Santa Rosa, CA
   Regulatory Affairs Specialist, Medtronic Vascular, Santa Rosa, CA
   Quality Assurance, W. L. Gore & Associates, Inc., Flagstaff, AZ
   Regulatory Affairs Associate, W. L. Gore & Associates, Inc., 
Flagstaff, AZ
   Director, Quality Assurance & Regulatory Compliance, Myogen, Westminster,
CO
   Research Quality and Compliance Auditor (Clinical), US Oncology, Houston,
TX


Featured Conference:

16th International Contracting & Negotiating Clinical Trials
San Diego, CA   September 19-20, 2005
The 16th International Contracting & Negotiating Clinical Trials conference
organized by Strategic Research Institute in association with MAGI (Model
Agreement Group Initiative) is organized to bring together the senior-level
decision makers from the Sponsor, CRO and Site communities to present
high-quality, on-topic presentations that deliver nuts-and-bolts advice and
real-life stories.  For more information, phone (212) 967-0095 or visit
www.srinstitute.com/cs337.

To view in-depth information about the above opportunities -- including
contact information -- please visit the JobWatch section of the CenterWatch
web site (http://www.centerwatch.com/careers/careers.html).

Thank you, and we hope you find this information helpful.

CenterWatch
http://www.centerwatch.com





-- 
--  Esther L.,  esther-L at mailsnare.net or esther-L at alumni.virginia.edu
Speaking only for myself