The Origin Group Ltd (TOGL) is seeking a Study Monitor/Clinical Research Associate to oversee clinical studies in line with approved protocols, GCP and sponsor SOPs. You will monitor sites, protect participants and ensure data integrity across UK studies.
Reporting to the Head of Clinical Operations, you will conduct site visits (remote or on-site), review informed consent and source data, manage trial documentation, and escalate issues to keep studies on track while upholding high standards and
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Clinical Research Associate - Remote & Onsite Monitoring employer: Camwebdir
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