Natalie Sommerville

Clinical Research Associate @Medpace

Essential duties are as follows-Ensure site compliance while conducting qualification, study initiation, routine monitoring, and study close-out visits for research sites according to Medpace/Sponsor Standard Operating Procedures (SOPs)-Serve as a primary resource to the clinical investigator and site staff -Maintain close collaboration, interaction, and effective working relationships with Medpace internal cross-function teams -Verify that the rights and well-being of subjects are protected, the reported trial data are accurate, complete and verifiable from source documents, and the conduct of the trial is in compliance with the currently approved protocol/amendment(s), GCP, and applicable regulatory requirements -Ensure quality completion of visit reports, follow-up letters, and maintenance of study-related databases and ClinTrak Monitoring Portal.