Senior Clinical Research Associate
CurrentProvides overall site management for Phase I-IIIB clinical studies that encompasses the following: subject safety, protocol overview/training, data review for the assurance of data integrity, query resolution, TMF/ISF reconciliation, drug accountability, issue management, and ensuring the compliance of all sites. Responsible for qualifying, initiating, monitoring, and closing out sites participating on studies. Responsible for completing a comprehensive Trip Report relevant to the site visit. Provides excellent communication to the sites and study team. Adheres to the companies SOP's, GCP Guidelines, and Ethical Standards.
Apr 2016 - Present
