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Date:         Wed, 25 Jul 2001 08:30:25 -0700
Reply-To:     Jeff Neubert <techni_pro@YAHOO.COM>
Sender:       "SAS(r) Discussion" <SAS-L@LISTSERV.UGA.EDU>
From:         Jeff Neubert <techni_pro@YAHOO.COM>
Subject:      ANOTHER SAS Job - No. NJ
Content-Type: text/plain; charset=us-ascii

Techni Pro is a small consulting company that pays you a high percentage of YOUR bill rate.

One contract position currently exists at a large pharmaceutical company in North New Jersey.

Please send resume to Jeff Neubert Techni_Pro@Yahoo.com

Rate: $58/hr W-2 only (possible sponsorship)

Length: 12 months estimated.

Description: Provide statistical programming support and validation, and help set specifications of analysis datasets , pooled datasets, statistical tables, summaries, figures and listings for Phase II-IV clinical trials related to efficacy in BRAID (Bone/Respiratory/Arthritis/Infectious diseases/Dermatology) and CMEG (Cardiovascular/Metabolic/Endocrine/Gastrointestinal) studies. Employ standardized programs where applicable. Provide input into planning documents such as protocol, validation plan, and report and analysis plan. Provide outputs for clinical study reports, integrated summaries, and electronic submissions. Help respond to health authority inquiries for submitted dossiers. Establish and maintain sound working relationship and effective communications within Biostatistics and Statistical Programming, and Clinical Research BRAID/CMEG.

Skills Required: BA/BS or equivalent experience in computer science, mathematics, statistics, life sciences, or related field(s). Intermediate SAS programming skills, with 2-5 years experience in a medical setting, preferably working with clinical trials data. Good understanding of clinical trial practices, procedures and methodologies. Good verbal and written communication skills. Good interpersonal and organizational skills. Attention to detail and correctness. Working knowledge of office tools. MS in Statistics is a plus.

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