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The Cyber-Spy.Com Usenet Archive Feeds Directly From The Open And Publicly Available Newsgroups These Group And Thousands Of Others Are Available On Most IS NNTP News Servers On Port 119. Cyber-Spy.Com Is NOT Responsible For Any Topic, Opinions Or Content Posted To These Or Any Other Newsgroups. This Web Archive Of The Newsgroups And Posts Are For Informational Purposes Only. Message-Id: <03120903310714.NP17341@jobcircle.com> Newsgroups: alt.bestjobsusa.jobs.offered From: recruiter@jobcircle.com (JobCircle.Com) Reply-To: recruiter@jobcircle.com Subject: US-NJ: Edison-REGULATORY AFFAIRS ASSOC DIR Date: Tue, 09 Dec 2003 03:29:17 GMT NNTP-Posting-Host: 207.106.112.162 NNTP-Posting-Date: Mon, 08 Dec 2003 22:29:17 EST 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 !!! ************************************************************** Job Title: REGULATORY AFFAIRS ASSOC DIR Job Location: NJ: Edison Pay Rate: 100,000 - 140,0 Job Length: full time Start Date: 2003-12-08 Company Name: The Judge Group, Inc. Contact: Donna Dwulet Phone: 732-346-9100 Fax: 732-346-9101 Description: Major pharmaceutical company based in New Jersey seeks Associate Director Regulatory affairs.The Associate Director of regulatory affairs is the DRA representative responsible for assuring the regulatory integrity of assigned investigational and marketed products. This associate is the primary liaison with FDA, interacting with FDA officials. This associate will be the sole DRA representative on assigned international project teams, and will obtain input from regulatory associates in key affiliated companies. The Assoc. Director is responsible for designing and implementing registration strategies for assigned compounds that will lead to optimal worldwide registration and will review and assesses the accuracy and appropriateness of all submissions to the FDA and/or major documents to foreign health authorities. The Assoc. Director will coordinate all meetings with the FDA and will assist in clearance of promotional materials. Minimum Requirements: Strong knowledge of US regulatory affairs and FDA regulations and good understanding of the drug development process is required. Candidates must possess a Ph.D. in a biomedical science, Pharm.D., or equivalent and must have 4-6 years experience in regulatory affairs. Knowledge of EU or Asian regulatory affairs is desirable and will place the candidate at a significant advantage. Strong interpersonal, oral and written communication skills are mandatory for effective interactions with worldwide and regulatory authorities. Knowledge of international drug development process and computer skills are highly desirable. The determination of the Associate director level will be made based on the candidates experience and knowledge of regulatory affairs, drug development or equivalent. Please refer to Job code JO031992 when responding to this ad. For FASTEST PROCESSING of your resume, please visit http://www.jobcircle.com/classifieds/445060.html to apply online. ************************************************************** For fastest processing of your resume, this employer asks that you apply to this job using the URL above. ************************************************************** Go Back To The Cyber-Spy.Com Usenet Web Archive Index Of The alt.bestjobsusa.jobs.offered Newsgroup |
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