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/iframe></center><br><br> <br><br> </center> </td></tr> </table> <center> <table> <tr><td width="600"><center><hr width="400"><font size="2"><b>The <a href="http://www.cyber-spy.com/">Cyber-Spy.Com</a> Usenet Archive Feeds Directly<br>From The Open And Publicly Available Newsgroups<br><br>These Group And Thousands Of Others Are Available<br>On Most IS NNTP News Servers On Port 119.<br><br><a href="http://www.cyber-spy.com/">Cyber-Spy.Com</a> Is NOT Responsible For Any Topic,<br>Opinions Or Content Posted To These Or Any Other<br>Newsgroups. This Web Archive Of The Newsgroups And<br>Posts Are For Informational Purposes Only.<br><br></b></font><hr width="400"></center><center><font size="2"><pre><b> Message-Id: <03102021041357.NP16449@jobcircle.com> Newsgroups: alt.bestjobsusa.jobs.offered From: wyeth@trackcareers.com (JobCircle.Com) Reply-To: wyeth@trackcareers.com Subject: US-PA: Collegeville-Associate Director II, Regulatory Affair Date: Mon, 20 Oct 2003 21:02:23 GMT NNTP-Posting-Host: 207.106.112.162 NNTP-Posting-Date: Mon, 20 Oct 2003 17:02:23 EDT Organization: JobCircle.com (jobcircle.com) ************************************************************** JobCircle.com - Careers, Content and Community for Technology professionals in the Northeastern United States! Jobcircle.com provides resume submission, classified searches, eLearning, hundreds of career development articles, tech news, and more to tens of thousands of Technology professionals in your area - visit us today at http://www.jobcircle.com! !!! Voted a TOP 50 Career Web Site in 2002 by CareerXRoads !!! ************************************************************** Please reply to wyeth@trackcareers.com with your resume! Job Title: Associate Director II, Regulatory Affair Job Location: PA: Collegeville Pay Rate: Open Job Length: full time Start Date: 2003-10-20 Company Name: Wyeth Pharmaceuticals Contact: Wyeth Phone: xxx-xxx-xxxx Fax: xxx-xxx-xxxx Description: The Inflammation Therapeutic Area of Wyeth Research includes such key marketed products as the breakthrough rheumatoid arthritis therapy Enbrel, the transplant immunosuppressant Rapamune, both of which are under continued development in new or expnaded indications; and a number of promising new development projects for rheumatoid arthritis, osteoarthritis, analgesia, asthma and bone fracture healing. As Associate Director II, Regulatory Affairs, in the Inflammation Therapeutic Area of Global Product Development, you will be responsible for planning and implementing the global regulatory strategy, and managing regulatory submissions throughout development, from first in man clinical studies through to marketing applications, for defined projects. You will be the Regulatory Affairs representative to the Global Development and Global Strategy Teams and the lead of the Global Regulatory Team on each assigned project. You will be responsible for interfacing directly with government regulatory personnel, including scientific reviewers and administrative staff, and Wyeth affiliate staff in all markets to facilitate and coordinate regulatory objectives; this includes negotiating complex regulatory issues pertaining to product development and planned regulatory submissions or those under review. You will be responsible for providing interpretative analysis of regulatory guidance documents, regulations, or directives that impact Wyeth projects or products, and ensuring personnel in other departments are advised of their applicability and impact. In addition to strategic and operational responsibilities as Global Regulatory Team lead, you will direct the professional growth of subordinates (both professional and administrative) by providing individualized guidance, mentoring, and supervision relative to their job responsibilities and capabilities. You will also ensure that the staff operates effectively in the department and company team environment. This includes building and maintaining a good team environment with staff and personnel in other departments. This position requires a B.S. or M.S. degree in a biological science; a PharmD or Ph.D. is desirable. Applicants must have a minimum of 6 - 8 years regulatory experience in a research orientated pharmaceutical company. Previous regulatory agency experience would be advantageous, and management or supervisory experience is desirable. Applicant must be a U.S. resident or currently able to legally work in the U.S. Please refer to Job code R900259 when responding to this ad. For FASTEST PROCESSING of your resume, please visit http://www.jobcircle.com/classifieds/444057.html to apply online. ************************************************************** For fastest processing of your resume, this employer asks that you apply to this job using the URL above. ************************************************************** </b></pre></font><hr width=650><a href=http://www.cyber-spy.com/alt.bestjobsusa.jobs.offered-index.html><font size=3>Go Back To The <a href=http://www.cyber-spy.com/>Cyber-Spy.Com</a><br>Usenet Web Archive Index Of<br>The alt.bestjobsusa.jobs.offered Newsgroup</font></a><br><br></center></td><img src=http://cyber-spy.com/cgi-bin/livecntr.pl?0+1+unetjobs width=1 height=1> </tr> </table> </center> <center> <br><center><hr size="3"></center> <table width="100%" cellpadding="0" border="0" cellspacing="0"> <tr> <td align="left" valign="top"><small><b><i><a href="http://www.cyber-spy.com/index.html">Cyber-Spy.Com Live Resources</a></i></b></small></td> <td align="right" valign="top"><small> Copyright Alpha Omega Delta,<br> All rights reserved. </small></td> </tr> </table> <center><hr size="3"></center> <br><br> <br><br></center> </body></html>