Clinical Research Associate - Oncology & Monitoring

We are in search of an experienced Clinical Research Associate to conduct on-site and in-house monitoring to verify that the rights and well-being of human subjects are protected, reported trial data is accurate and complete and verifiable from source documents, and ensure the trial is conducted in compliance with the currently approved protocol, Good Clinical Practices, ICH Guidelines and FDA regulations.
REQUIREMENTS
·Conduct pre-study site visits to evaluate adequacy of site, investigator and research staff
·Provide on-site orientation of Investigators and other site personnel
·Conduct ongoing monitoring visits to assigned investigational sites to verify that the rights and well-being of human subjects are protected, the reported trial data are accurate, complete and verifiable from source documents
·Ensure that study documentation is completely and properly maintained
·Prepare and submit timely appropriate monitoring forms and site visit reports
·Monitor Investigator compliance for the reporting of Adverse Events and Serious Adverse Events
·Lead Project Team meetings

e-mail resume to [Click here for email]

www.beckerstaffing.com