Sr. Qualification Engineer (Germany) - 2 year assignment available International
3/26/2015 7:56 AM

In this role you will be responsible for carrying out Installation, Operational and Performance Qualification of new and modified production facilities, equipment, utilities, and computerized systems in order to demonstrate that the system is fit for its intended use, and repeatedly and reproducibly meets critical requirements. For U.S. canddiates we are open to a 2 year assignment   ...View Job
Associate Director/Director (Senior), Oncology California
3/12/2015 2:31 PM

Provide clinical oversight for one or more oncology projects and will work with a cross functional team to plan, develop, design, implement and complete clinical development (Phase I to 3) studies. This position will have accountability for medical monitoring, analysis, and reporting of studies. The oncology programs will involve interactions and developing strategic relationships with resea  ...View Job
Specialist/Sr. Specialist/Manager Quality GCP Compliance California
3/10/2015 2:33 PM

Are you a clinical professional looking to expand your experience and broaden your career horizon? This is the position for you – utilize your clinical experience in the Quality arena. PRIMARY PURPOSE OF POSITION: This QA position is a member of the Quality team and provides QA support and oversight to ensure compliance with Good Clinical Practice (GCP). Areas of responsibilities include, bu  ...View Job
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