Associate Director, Document Control Clinical California
3/3/2015 4:08 PM

Overview: Provide leadership and management oversight of clinical document control and clinical training. Partner with Clinical Development, Quality Assurance, and Regulatory Affairs to enable the development and maintenance of Standard Operating Procedures (SOPs) and clinical documents. Ensures Clinical Development is appropriately trained on SOPs. Manage and oversee the team responsible for  ...View Job
Clinical Trial Manager - Asthma California
3/3/2015 4:06 PM

Overview: Responsible for managing the full scope of proper study conduct including, but not limited too, protocol development to final report, regulatory filing and/or publications, coordinating cross functional efforts in the administration and progress of Phase 1 to 4 clinical trials. Additional responsibilities include trial start-up, conduct, and close-out activities in order to achieve pr  ...View Job
Senior, Clinical Research Associate - Monitoring California
3/3/2015 4:04 PM

Overview: Manage assigned activities of clinical study to ensure it is completed on time, within budget, and in compliance with Good Clinical Practice (GCP), government regulations, and overall clinical objectives. Responsible for quality study oversight, including but not limited to monitoring, oversee clinical vendors and Regional Monitors, and review monitoring trip reports. Participate in t  ...View Job
Clinical Trial Manager/Sr. CTM - Oncology California
3/3/2015 4:01 PM

Overview: Manage and lead all aspects of one or more Oncology Phase 1 to 4 clinical trials including, but not limited to protocol development to final report, clinical operations support for trial start-up, conduct, and close-out activities in order to achieve program objectives and goals. Collaborate with Clinical Contracts/Budget to manage efforts for clinical service provider selection.   ...View Job
Director/Sr. Director, Commercial Quality Assurance California
3/3/2015 2:45 PM

This position will have oversight and leadership of quality systems and programs to meet compliance, validation, quality assurance requirements, which range from Good Laboratory Practices (GLP) to Good Manufacturing Practices (GMP). * Build and maintain robust quality program that will effectively support the various phases of drug development – preclinical to commercial launch. * Pro  ...View Job