SCOPE: Plan, develop, and implement the activities of the Document Management and Control Department, which maintains designated cGMP documents and document management processes RESPONSIBILITIES: ? Supervise, coordinate, and prioritize the daily activities of the Document
2/1/2012 Durham, NC Save This JobSCOPE: This individual will be carrying out research and/or development work to support understanding of immunotherapy product mechanism of action. The product is currently undergoing testing in clinical trials. RESPONSIBILITIES: ? Participate in the development of methods and
2/1/2012 Durham, NC Save This JobKAI Pharmaceuticals, located in South San Francisco, is a clinical-stage, biopharmaceutical company whose lead peptide product candidate, KAI-4169, is in development for the treatment of chronic kidney disease-mineral and bone disorder (CKD-MBD). Building on promising,
1/26/2012 South San Francisco, CA Save This JobJob Purpose: The Clinical Trial Associate (CTA) is responsible for logistical and tactical activities related to study management in partnership with Program Managers, clinical trial managers and lead clinical research associates. This position offers a career pathway to a
12/18/2011 Bannockburn, IL Save This JobJob Purpose: Independently organize and manage multiple tasks related to clinical development programs of varying type and complexity; while simultaneously ensuring study milestones are met and completed according to the protocol, regulatory requirements and Cytochroma
12/18/2011 Bannockburn, IL Save This JobJob Purpose: Through partnership with Clinical Services and other functions, GCP QA operations is responsible for ensuring high quality clinical trails are performed in compliance with worldwide regulatory expectation. Under the direction of the Director of Quality
12/18/2011 Bannockburn, IL Save This Job
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