Senior Clinical Research Associate

The Senior Clinical Research Associate (Sr. CRA) plays an integral part in the successful monitoring and management of clinical trials. Responsibilities of a Sr. CRA include ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. Sr. CRAs may be required to travel up to 65%. Monitor clinical studies of investigational and approved products that have been determined to satisfy a medical need and/or offer a commercial benefit, including qualification, initiation, interim, and close-out site visits. Manage and train site personnel on therapeutic area, protocol requirements, proper source documentation, and case report form completion. Serve as a resource for project team members including supporting CRA I and CRA II staff by providing solutions to resolve issues.