Occupation:Clinical Research |
Location:Jacksonville, FL |
Education Level:Bachelor |
Will Relocate:YES |
Description
Responsibilities included Clinical study monitor responsible for: * Performing clinical study visits clinical studies and ensuring compliance with ICH/GCP guidelines, FDA guidelines and Sponsor SOPs * Ensuring safety of all clinical study patients * Ensuring data integrity through source-document verification of key study data * Supervision of clinical study monitors including assistance with study closeout * Entry/completion of study data * Ensured completion of clinical study timesheets * Reviewed expense reports of clinical study staff Clinical study monitor responsible for: * Monitored activities at clinical study sites to assure adherence to Good Clinical Practices SOP's and study protocols Review regulatory documents. * Maintain awareness of developments in the field of clinical research as needed.
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