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Manage tracking of clinical study related activities with accuracy and proficiency according to regulatory standards. Strong organizational and time management skills including the ability to work independently and multi-task. Perform and maintain surveillance and oversight of12/30/2013 Durham, NC Save This Job
Participate and contribute as an innovative project team member supporting and facilitating the management of one or more global clinical trials in accordance with GCP/ICH guidelines and local/country regulatory requirements. Accountable to provide quality and effective document11/30/2013 Durham, NC Save This Job
Responsible for all aspects of one or more global clinical trials from the preparation, execution, and reporting associated with clinical trials in accordance with GCP/ICH guidelines and local/country regulatory requirements. Facilitation and coordination and full project11/30/2013 Durham, NC Save This Job
Responsible for design, conduct, analysis, interpretation, reporting and presentation of clinical pharmacology studies for products under development. Studies may include first-in-human, proof-of-concept, drug interaction, special population, bioequivalence, mass balance and QT11/30/2013 Durham, NC Save This Job