Clinical Research Specialist/Nurse-Research and Education Institute
Knowledge of Federal and State regulations and International Guidelines related to Good Clinical Practices in clinical research....
As the clinical research specialist, you will be responsible for assisting with study planning, starting up and executing studies, gathering clinical data, and performing data analysis....
Clinical Research Associate (Home Based) - part-time
to the study protocol and in accordance with SOPs, applicable regulations and the principles of Good Clinical Practice....
Remote WorkIn-House Clinical Research Associate (no travel)
The job Provide leadership and guidance to Clinical Research team. Participate in clinical research site management, qualification, initiation, interim monitoring, and study close out....
OVERVIEW We are currently searching for a skilled professional to join a well-known client’s team as a Senior Clinical Research Associate in San Francisco, California....
Clinical Research Associate Location: South San Francisco Department: Clinical Development Description The Position Clinical Research Associate (CRA) assists with the management of Veracyte's clinical...
Senior Data Safety Monitor (Clinical Research Associate)
These monitoring/auditing visits will be conducted according to Good Clinical Practice (GCP), the Code of Federal Regulations (CFR), the UCSF IRB, and the UCSF DSMP....
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Senior Data Safety Monitor (Clinical Research Associate)
Reuters is looking for a scoop-hungry Technology Correspondent to follow the money and characters in Silicon Valley funding the technology that will change our future.The successful candidate will...
Clinical Research Associate - Field Management
all monitoring and site management activities....
Senior Clinical Research Associate
The Senior Clinical Research Associate (CRA) is responsible for management and monitoring activities that will lead to successful execution of clinical studies....
Clinical Research Associate - Field Management - West
all monitoring and site management activities....
operational milestones An understanding and demonstrated application of Good Clinical Practices and ICH Guidelines is a plus....
Clinical Research Associate (CRA) - B
Manages the essential documents, as required by local regulations and ICH GCP, before, during and after a clinical trial....
R&D: Senior Clinical Research Associate
Experience in a clinical research environment, preferably in medical device and/or dermatology or aesthetic space, that includes hands-on site management for clinical trials....
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Everything we do in healthcare has to be discovered and thoroughly tested before it can be put into practice. In this course, you will explore clinical research its challenges and its huge...
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