Clinical Research Coordinator
Current• Completed forms, correspondence, and reports to the CROs and sponsors promptly• Created tools to ensure protocol compliance and compliance with the requirements ofregulatory agencies• Responsible for ensuring completeness of CRFs and developing study-specific case report forms• Ensured prompt reporting of Adverse Events and Serious Adverse events• Identified problems/inconsistencies within the source documentation andrecommended corrective action as appropriate•… Show more • Completed forms, correspondence, and reports to the CROs and sponsors promptly• Created tools to ensure protocol compliance and compliance with the requirements ofregulatory agencies• Responsible for ensuring completeness of CRFs and developing study-specific case report forms• Ensured prompt reporting of Adverse Events and Serious Adverse events• Identified problems/inconsistencies within the source documentation andrecommended corrective action as appropriate• Screened patients for study eligibility per the inclusion/ exclusion criteria found inthe protocol and executed the informed consent process• Managed Processing and Shipment of Lab Samples Show less