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This CRA will be primarily responsible for ensuring site compliance with specified research protocols and the accuracy of submitted data. The CRA will also be responsible for maintaining proper written documentation for the study records of all site10/22/2014 Burlington, MA Save This Job
Description: Job Summary Responsible for the planning, implementation and conduct of global clinical trials in a fast paced oncology focused company. Provide operational leadership and ensure the successful implementation of multiple global Phase 2 clinical development programs.10/14/2014 Redwood City, CA Save This Job
Description The Clinical Research Associate (CRA) assists in monitoring and completion of high quality, Class III medical device clinical trials. This position will be a primary contact with medical professionals involved in clinical studies. Must be enthusiastic, positive and9/22/2014 Audubon, PA Save This Job