Friday, May 25, 2012

Takeda Makes Another $266.3M Buy; Pfizer Drug Confuses FDA Panel - May 25, 2012

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Top Stories 
•  Takeda Pharmaceutical Co. Ltd. (TKDG.DE) Makes Another $266.3 Million Buy More...
•   Pfizer Inc. (PFE) Drug Confuses FDA Panel More...
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•  Eli Lilly and Company (LLY): Type 2 Diabetes Drug Safe and Effective in African Americans in Phase III Study More...
•  European Medicines Evaluation Agency Confirms Boehringer Ingelheim Corporation's Pradaxa Benefits, But Wants Clearer Guidance More...
•  GlaxoSmithKline (GSK) Diabetes Drug Data Revealed Amid Hostile Takeover More...
•  Elan Pharmaceuticals (ELN) Hoping Alzheimer's Drug Will "Transform" Firm More...
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University of Maryland Workshops in Biopharmaceutical Production: June 4-8, 2012

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Will be a critical individual contributor in a growing Medical Scientific Affairs (MSA) organization. The incumbent will serve a Publications Manager role, responsible for driving pull through of a complex medical communication plan for Ironwood's first product, plus future products, and will also serve as the Grants Coordinator for Investigator-Initiated and Collaborative external research supported by Ironwood.

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Gen-Probe Incorporated
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Responsible for assisting scientific staff in carrying out research assignments involving a variety of laboratory methods, equipment and procedures. Duties: Conducts moderately complex laboratory bench experiments. Participates in experimental design, analysis and organization of data for presentation etc.

Rocky Bio (Salt Lake City, Utah)

Watson Pharmaceuticals, Inc.
Scientist Senior
Participates as a team member in method development and validation and complex technical investigation efforts, performs highly technical and specialized Analytical Scientist duties, research on assigned problems and studies in support of Watson̢۪s efforts.

BioTechxus (Houston, Texas)

Pfizer Inc.
Director/Senior Director, Regional Medical & Research Specialist
Responsible for providing clinical and research support for the therapeutic area in the region. The RMRS role is to enhance medical communication between Pfizer and therapeutic experts and researchers, support clinical and outcomes research development, facilitate research site selection and study placement, and assist with the support of both Pfizer sponsored and investigator initiated research activities.

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