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<html xmlns:o="urn:schemas-microsoft-com:office:office" xmlns:w="urn:schemas-microsoft-com:office:word" xmlns="http://www.w3.org/TR/REC-html40"> <head> <META HTTP-EQUIV="Content-Type" CONTENT="text/html; charset=Windows-1252"> <meta name=ProgId content=Word.Document> <meta name=Generator content="Microsoft Word 9"> <meta name=Originator content="Microsoft Word 9"> <link rel=File-List href="cid:filelist.xml@01BFED60.28FEE520"> <title>Associate Director Ц Clinical Screening Laboratory</title>  <style>  </style> </head> <body lang=EN-US link=blue vlink=purple style='tab-interval:.5in'> <div class=Section1> <h2>Associate Director, Clinical Sample Analysis/Pharmacokinetics<o:p></o:p></h2> <![if !supportEmptyParas]> <![endif]><o:p></o:p> <h1>Reference: #1068аа <o:p></o:p></h1> <h1><![if !supportEmptyParas]> <![endif]><o:p></o:p></h1> We are seeking an experienced manager to lead a team of 10 Ц 13 scientists in the development and execution of assays for the evaluation of samples collected during clinical studies.а The candidate will interact closely with the clinical department to assess the assay requirements for different clinical programs, and will report issues that may affect results and timelines.а This individual will actively participate in the design and development of appropriate clinical assays, and the adaptation of assays developed in the research and development departments for use by the clinical testing laboratory.ааа In addition, he/she will oversee the operations of the clinical testing laboratory which is responsible for the receipt, distribution, and analysis of clinical samples, and data reporting to the clinical department.а The selected candidate will be a proven leader capable of interacting productively with members of the clinical, research, development, and regulatory staff with the goal of generating clinical laboratory data of the highest quality.а <![if !supportEmptyParas]> <![endif]><o:p></o:p> Requirements: заа Ph.D. in Pharmacology, Immunology, Molecular Biology, Biochemistry or related discipline. з а At least 3 years of experience in the evaluation of clinical samples (serum, saliva, genital tract secretions, etc.). з а Previous experience designing and developing pharmacodynamic and pharmacokinetic assays, primarily for antibody and polypeptide drugs is required. з ааааааа Demonstrated expertise with state-of-the-art techniques for the detection and quantitation of antibodies and bioactive polypeptides in clinical samples is also required.а з а Some familiarity with current molecular biology techniques and FACS-based assays is desired.а з а Excellent oral and written communication skills are a must.а <![if !supportEmptyParas]> <![endif]><o:p></o:p> Our client has therapeutics and vaccines in the market and a strong pipeline of products in various stages of development and clinical trials. <![if !supportEmptyParas]> <![endif]><o:p></o:p> If you have an interest in this or other opportunities, please email your resume as an attached file to the attention of Ann G. Rathbun, Managing Director.а If necessary, send by FAX or surface mail. <![if !supportEmptyParas]> <![endif]><o:p></o:p> Rathbun, Sapir & Associates P.O. Box 2337 Sedona, AZ 86339-2337 (520) 203-0074 Telа (520) 203-0075 FAX <a href="mailto:rathbun@sedona.net">rathbun@sedona.net</a> EMail </div> </body> </html>

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