Clinical Research Regulatory Coordinator I — Study Start-Up

A leading medical institution in Florida is seeking a Clinical Research Regulatory Coordinator I to manage regulatory files for pediatric clinical research studies. The role involves coordinating IRB submissions and preparing necessary regulatory binders. The ideal candidate should have a Bachelor's degree with at least 2 years of relevant experience, or an Associate's degree with 6 years of experience. Strong organizational and communication skills are essential in this temporary, grant-funded role. #J-18808-Ljbffr