Director, Quality Assurance California-Silicon Valley/Peninsula
4/17/2015 11:29 AM

Directs the development, implementation and maintenance of quality assurance systems and activities. Directs generation and review of documents used in Good Manufacturing Practices. Also directs internal and external audits for GMP activities. May audit raw material vendors and prepares manufacturing documentation for updated filings. Coordinates inter-department day to day QA activities. Lead inv  ...View Job
Clinical Trial Manager California-San Francisco
4/17/2015 11:19 AM

The Clinical Trial Manager will manage all components of a clinical trial, leading a multidisciplinary, cross-functional Study Management Team. The Clinical Trial Manager is accountable for ensuring clinical trial activities and deliverables are completed on-time, within budget, and in a highly dynamic and complex environment in accordance with appropriate quality standards including GCP/ICH requ  ...View Job
Clinical Contracts Manager California
4/15/2015 11:47 AM

Manages the negotiating, structuring, and management of contractual documents that establish business relationships with vendors, customers and/or partners. Reviews and approves documents for protection of the company's contractual posture and adherence to company policy. Advises management of contractual rights and obligations and provides interpretation of terms and conditions. May select, deve  ...View Job
Staff Scientist, Translational Modeling & Simulation California-San Francisco
4/9/2015 1:47 PM

Develops predictive models using the PBPK approach to address drug-discovery and development questions pertaining to different therapeutic areas with a focus on pain management and oncology. Works in close partnerships across various functions including Research, Preclinical and Clinical Development, Biostatistics, and Regulatory. This job contributes to and supports the company's research and   ...View Job
Manager, Medical Writing California-San Francisco
3/24/2015 3:48 PM

Responsible for supporting Clinical Development Lead in clinical protocol development, clinical study reports, Investigator's Brochures, IND/NDA. Responsible for researching, writing and editing clinical reports, summarizing data from clinical studies for submissions to the FDA and for publication and/or presentation and ensures documents are written in compliance with all regulations (ICH, GLP  ...View Job