URGENT OPPORTUNITY – GCP Auditor – Europe – 100% Remote – 6 Months ContractJob Title:GCP AuditorStart Date:ASAPLocation:Europe (100% Remote)Language:Ideally German speakers but English speakers are also welcome.Job DescriptionConduct GCP audits of investigator sites, sponsors, CROs, and vendors involved in clinical trials.Ensure compliance with ICH-GCP E6 Guidelines and applicable European regulations.Review essential trial documentation including Trial Master Files (TMF), Investigator Site Files (ISF), protocols, and informed consent forms.Verify the accuracy, completeness, and traceability of clinical trial data.Identify compliance risks, protocol deviations, and areas for improvement during audits.Prepare detailed audit reports and communicate findings to clinical and quality teams.Support the implementation and follow-up of Corrective and Preventive Actions (CAPA).Ensure readiness for regulatory inspections from authorities such as the European Medicines Agency and national competent authorities.If you are interested in this position, please send your updated CV by email to, specifying your availability and phone number so we can connect quickly.#J-*****-Ljbffr