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Job Summary: The Associate Director should possess a strong in vitro and in vivo pharmacology background combined with significant drug development experience. The Associate Director will have the opportunity to work across multiple therapeutic areas including CNS, fibrosis,8/11/2014 Lexington, MA Save This Job
SUMMARY: The Senior Director of Regulatory Affairs reports directly to the Executive Director, Regulatory Affairs. This position coordinates departmental planning, manages multiple project teams and provides the regulatory strategies to ensure appropriate implementation of key8/16/2014 Redwood City, CA Save This Job
Job Summary The Associate Director, Drug Metabolism & Pharmacokinetics (DMPK) is responsible for. the nonclinical assessment of New Chemical Entities, which includes lead optimization, ADME, PK/ PD, modeling and simulation, GLP bioanalysis, and CRO management of pharmaceutical9/30/2014 Palo Alto, CA Save This Job
Director, Target Discovery & Validation Location: South San Francisco, CADepartment: Research & DevelopmentType: Full TimeMin. Experience: Senior Manager/Supervisor General Description: Second Genome is seeking an energetic and creative individual with experience in novel target9/30/2014 South San Francisco, CA Save This Job
Director, Clinical Operations DEPARTMENT/GROUPClinical OperationsLOCATIONSan Francisco, CA% TRAVEL REQUIREDUp to 25% Description Responsible for clinical operation timelines, and planning activities for each clinical study. Directs and manages the overall execution of clinical10/2/2014 San Francisco, CA Save This Job
Description: Reporting to the Senior Director of Toxicology, the successful incumbent will have at least 5 years of experience in preclinical drug development with emphasis in toxicology and preclinical safety; experience on drug development project teams would be a plus;9/3/2014 San Francisco, CA Save This Job