Clinical Research Coordinator
CurrentQA multiple problem trials and successfully returned to excellent standing with the CRO.Complete all forms and correspondence and reports to the CROs and sponsors in a timely manner.Primary responsibility to screen, enroll and follow study subjects ensuring protocolcompliance and close monitoring while the subjects are on the study. Responsible for all data collection, source documentation, developing/completing study.specific case report forms and submission of adverse experience reports. Creating study specific tools for source documentation when not provided by the sponsor.Ensuring compliance with protocol guidelines and requirements of regulatory agencies;identify problems and/or Inconsistencies and monitor patients progress to includedocumentation and reporting of adverse events; recommend corrective action as appropriate.Initiated studies, screened patients for study eligibility to participate as per protocol, inclusion exclusion criteria and informed consent process Created a system of organization for eligible patients.
