Subj : Clinical Research Associate in Biotech----------------------------- To : All From : sqafyi@yahoo.com Date : Thu Jan 31 2019 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) .