The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.
Job listings
As a Principal CRA, you will be joining the world’s largest & most comprehensive clinical research organisation. Responsibilities include study specific training, developing and updating monitoring tools, contributing to study monitoring updates, site visits, trip report review, document management, issue escalation, and data facilitation. It is a Lead CRA position with partial project management.