Wednesday, February 29, 2012

FDA Adds New Warning to Statin Labels - Feb. 29, 2012

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ViroPharma Incorporated
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Follow established standards and procedures to provide a wide range of clinical programming duties including designing, developing, evaluating, and modifying SAS programs to analyze and evaluate clinical data.

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Clinical Research Associate
Conducts site qualification, site initiation, interim monitoring visits and study close-out visits. Monitors progress of subject enrollment. Performs source document verification of electronic Case Report Forms (eCRFs).

Biotech Bay (South San Francisco, California)

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Clinical Research Associate II
Contribute to the preparation of clinical protocols and amendments. Performs clinical study or clinical site feasibility. Assist in the activities associated with site start-up and management. Support the administration of study budgets.

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Clinical Data Manager
Identify external data issues and tracks resolutions. Reviews listings to identify data discrepancies and tracks resolutions. Performs database design and edit check specification testing.

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BioSpace Career Fair at CALBIO2012

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BioSpace Career Fair at CALBIO2012, San Francisco, CA March 7, 2012
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BioCapital Career Fair, Bethesda, MD April 25, 2012
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The world has radically changed in just the last few years and the trend is likely to continue at an exponential rate. Partnerships in Clinical Trials is changing with it. Partnerships has always been where business gets done and strategic partnership deals are inked, but in 2012 it is where the industry moves forward with answers. We've taken your most pressing challenges and translated them into the most provocative meeting agenda the industry has ever seen.

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