Bavisha Varma

Senior Clinical Research Associate @Medpace

Cincinnati, KY, US

Verify that the safety of research subjects are protected, that the reported trial data are complete, accurate, and verifiable from study source documents, and that the conduct of the trial is in compliance with the currently approved protocol, GCP guidelines, and applicable regulatory requirements.Serve as the primary Medpace resource for each clinical investigator and their site staff members.Maintain close collaboration, interaction, and effective working relationships with Medpace internal cross functional teams.Work as a fully independent CRA proficient in clinical monitoring and begin to initiate leadership roles as a member of the clinical operations teamTherapeutic Areas:Oncology (Primary)Endocrinology/MetabolicPediatrics/NeonatologyCardiology/Vascular Diseases

University of Cincinnati

Bachelor of Science (B.S.), Biological Sciences