URGENT OPPORTUNITY – GCP Auditor – Europe – 100% Remote – 6 Months Contract
Job Title: GCP Auditor
Start Date: ASAP
Location: Europe (100% Remote)
Language: Ideally German speakers but English speakers are also welcome.
Job Description
* Conduct 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.
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