Summit Clinical Research Solutions is seeking a detail-oriented professional to support the clinical research team in coordinating studies and ensuring regulatory compliance. The role involves assisting the clinical research coordinator and PI with study documents, submissions, and sponsor communications.The candidate will help prepare for monitor visits, update CTMS, and handle patient-related assessments while maintaining confidentiality and adherence to FDA, ICH GCP, HIPAA, and IRB#J-18808-Ljbffr