Our Clinical Monitoring & Operations team reviews clinical research data and ensures effective interaction with clinical trial sites throughout a clinical research study. This is conducted remotely and through on-site monitoring. Our focus is on innovation, continuous data review and risk-based quality management principles.
Our Clinical Research Associates (CRAs), Assistant Clinical Research Associates (ACRAs), Clinical Trial Coordinators (CTCs) and customer-dedicated teams oversee the protocols and efficacy of treatments during trials. We support the logistics and organization of clinical sites — ensuring that patients receive needed care, as well as identifying and treating clinical trial participants.