We are looking for a Clinical Research Associate III to join our Clinical Operations department. You will be based remotely in Italy.
You will be responsible for the setup of sites, budget proposals, and liaising with relevant authorities to ensure approvals are in place. Will be involved with more complex studies and challenging sites to monitor the progress of clinical trials onsite or remotely, to ensure the trials are conducted, documented and reported in accordance with the protocol, standard operating procedures (SOPs), all applicable regulatory requirements and ICH-GCP. Will work closely with sponsors, project managers and other members of the study team (CTLs) to ensure study deliverables are met within the project timelines.