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|    sqafyi@yahoo.com to All    |
|    Clinical Research Associate in Biotech--    |
|    31 Jan 19 19:19:45    |
      X-Received: by 10.224.59.205 with SMTP id m13mr364004qah.7.1369099003970;        Mon, 20 May 2013 18:16:43 -0700 (PDT)       X-Received: by 10.49.0.81 with SMTP id 17mr3339qec.16.1369099003821; Mon, 20        May 2013 18:16:43 -0700 (PDT)       Path:       eternal-september.org!mx05.eternal-september.org!feeder.eternal-september.org!n       ews.bbs-scene.org!border4.nntp.dca.giganews.com!border2.nntp.dca.giganews.com!n       ntp.giganews.com!ch1no54681qab.0!news-out.google.com!y6ni50601qax.0!nntp.google       .com!ch1no54678qab.0!postnews.google.com!glegroupsg2000goo.googlegroups.com!not       -for-mail       Newsgroups: dfw.jobs       Date: Mon, 20 May 2013 18:16:43 -0700 (PDT)       Complaints-To: groups-abuse@google.com       Injection-Info: glegroupsg2000goo.googlegroups.com; posting-host=72.85.190.129;        posting-account=j6gb_AoAAABpyJTCaie0cppupUobo2Hi       NNTP-Posting-Host: 72.85.190.129       User-Agent: G2/1.0       MIME-Version: 1.0       Message-ID: <74214cdf-f7bc-47ac-8cb1-cb0af9587eb3@googlegroups.com>       Subject: Clinical Research Associate in Biotech-----------------------------       From: sqafyi@yahoo.com       Injection-Date: Tue, 21 May 2013 01:16:43 +0000       Content-Type: text/plain; charset=windows-1252       Content-Transfer-Encoding: quoted-printable       Lines: 32       Xref: mx05.eternal-september.org dfw.jobs:250              Clinical Research Associate in Biotech       To apply for this position, please visit this Website.       http://biotech.fyicenter.com/jobs/99888805_Clinical_Research_Associate_in_Biote       ch.html       Date: 21-May-2013       To see other BioTech job opportunities, please visit       http://biotech.fyicenter.com/              Clinical Research Associate in Biotech              • Recruiting potential investigators, preparing EC submissions, translating       study-related documentation, organizing of meetings and other tasks as       instructed by supervisor; • Completing Serious Adverse Event (SAE) reporting,       processing production of reports;              • Assisting with training, mentoring, and development of new employees, e..g.       co-monitoring.              • Basic understanding of the clinical trial process • Minimum two years of       relevant clinical research experience in pharmaceutical or CRO industries •       Thorough knowledge of ICH Guidelines and GCP including a basic understanding of        regulatory requirements. • Thorough knowledge of monitoring procedures.              • University Degree (life science) or certification in a related allied health       profession from an appropriately accredited institution (e.g., nursing       certification, medical or laboratory technology); • Fluency in English       language.                     Thank you,       BioTech FYI Center       http://biotech.fyicenter.com/       --- Platinum Xpress/Win/WINServer v3.1        * Origin: Prison Board BBS Mesquite Tx //telnet.RDFIG.NET www. (1:124/5013)    |
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