• Participated in the management of assigned clinical trials. • Responsibilities included, abstracting, assembling, and organizing research data while monitoring the clinical course of patients entered onto research protocol.• Conducted Pre-study, Initiation, interim and Closeout Visits.• Implement and monitor clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH-GCP guidelines• Performed investigative site file reconciliation; requested any new or updated site-related essential and non-essential documents and reviews them for content, consistency with other documents, and compliance with appropriate local regulatory requirements, ICH guidelines, and project Standard Operating Procedures (SOPs), and sponsor requirements. • Maintains travel schedule at approximately 60-65%• Communicated common site trends to lead CRA and another project team member.• Worked closely with other team members to ensure timely resolution of project and/or clinical issues and obtained direction from more senior clinical operations staff.• Performed billable work in accordance with company policies, procedures, and Standard Operating Procedures• Provided regular clinical status information to team members and project management.• Monitored clinical trials to ensure sponsor and investigator obligations have been met and are compliant with applicable local regulatory requirements and ICH guidelines.• Visited sites to assess the qualification of potential investigative sites, initiated studies, instruct site personnel on the proper conduct of studies, to review data and ensure accuracy of data collected and to terminate studies. • Managed relationship with PI and study staff to ensure maximum productivity