Friday, May 04, 2012

Pfizer's Lyrica Fails Two Pain Studies - May 4, 2012

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•  Pfizer Inc. (PFE)'s Lyrica Fails Two Pain Studies More...
•  Raptor Pharmaceutical Inc. (RPTP)l Announces Publication of Phase 3 Results in the Clinical Journal of the American Society of Nephrology More...
•  Argos Therapeutics, Inc. Gets Encouraging Results from Study More...
•  CSL Behring Initiates Study of Subcutaneous Administration of C1-esterase Inhibitor in Patients with Hereditary Angioedema More...
•  Accentia Biopharmaceuticals (ABPI) Conducts Investigator Meeting in Preparation for New Multiple Sclerosis Drug Study for Cyrevia™ More...
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•  Alexza Pharmaceuticals, Inc. (ALXA) Slammed with a CRL for Adasuve™ More...
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•  Gentium S.p.A. Receives Day 180 List of Outstanding Issues From the CHMP for Defibrotide MAA More...
•  Immunomic Therapeutics Receives IND Authorization for Phase I Study of JRC-LAMP-Vax Vaccine to Treat Japanese Red Cedar (Sugi) Allergy More...
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•  Napo Pharmaceuticals, Inc. Comments on FDA Announcing Extension of Crofelemer NDA Priority Review More...
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•  Pfizer Inc. (PFE), Eli Lilly and Company (LLY) Help U.S. Test Failed Drugs for New Illness, National Institutes of Health (NIH) Reveals More...
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Events

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Top Jobs
Biotech Bay (Sunnyvale, California)

Pharmacyclics, Inc.
Clinical Research Associate/Senior Clinical Research Associate
Responsible for driving and executing day-to-day activities during the conduct of clinical studies, according to the protocol, ICH/GCP, and applicable regulatory requirements.

BioMidwest (Chicago, Illinois)

Takeda Pharmaceuticals
Medical Director / Senior Medical Director, Clinical Science
Leads the development of the all components of the integrated development strategy and the resultant tactical clinical plan and study designs to support the global development of and establish the conditions essential for determining the safety, efficacy, medical usefulness, and marketability of multiple compounds.

Southern Pharm (Memphis, Tennessee)

GTx, Inc.
Director, Clinical Development & Drug Safety
Responsible for managing the design and production of clinical protocols. Responsible for the development, implementation and execution of clinical development strategic plans that meet GCP, FDA, and other regulations or standards, and that are consistent with GTx business and function objectives

Biotech Beach (Inglewood, California)

ImaginAb, Inc.
Clinical Development Director
Supervise clinical research staff such as Clinical Study Managers (CSM), Assistant CSMs, and Data Managers. Will oversee all outsourced clinical research activities.

Rocky Bio (Salt Lake City, Utah)

Watson Pharmaceuticals, Inc.
Scientist Principal - Clinical Development
Plan, coordinate, and execute project-specific clinical research tasks related to the evaluation and development of new therapeutic products.

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Biotech Bay

Biotech Bay Career Fair

Job seekers can spend a day with HR representatives and Hiring Managers from top biotech, pharma, medical device and diagnostics companies in the Bay area.

Candidates with a 4-year degree in the life sciences and a minimum of 2-years of industry related experience are invited to attend. (Equivalent work experience may be considered in lieu of a four-year college degree. PhD and Postdoc candidates welcome.)

Exhibiting companies are recruiting for positions in areas such as: QA/QC, clinical research, engineering, manufacturing, biostatistics, clinical data management, chemistry, regulatory affairs, and research.

Job seekers may register here.

Biotech Bay Career Fair, Burlingame, CA May 29, 2012

More information about BioSpace's Career Fairs

BioSpace White Paper
Biotech Career Fairs For Job Seekers 101: Control Your Experience
By June Salvati, BioSpace Director of Events and Corporate Services
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•  Microbix Biosystems Inc. (MBXBF) Release: European Patent Office Revokes Controversial Patent More...
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•  Meda AB (MEDA-A.ST): Dymista - Could be the Drug of Choice More...
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Hot Company

Accelovance
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Accelovance Inc., based in Rockville, MD, is a clinical services company specializing in high patient throughput from recruitment through study completion. Accelovance has developed a model to increase the reliability and productivity on Phase I (outpatient) and Phase II-IV trials.

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