Clinical Research Associate

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Requirements

• Perform site monitoring visits
• Work with sites to adapt, drive, and track subject recruitment plan
• Administer protocol and related study training
• Evaluate the quality and integrity of study site practices
• Manage the progress of assigned studies
• Ensure copies/originals site documents are available for filing
• Create and maintain appropriate documentation regarding site management