Contract gcp auditor – investigator site audit dates:6th–7th april location:mexico engagement:short-term contract we are seeking an experiencedgcp auditorto conduct atwo-day investigator site auditinmexicoon6th–7th april, on behalf of one of our sponsor biotech clients. The audit will assess compliance with ich-gcp, applicable local regulations, and sponsor requirements. Key responsibilities: conduct a full investigator site audit in line with ich-gcp and local regulatory requirements review essential documents, isf, informed consent processes, imp management, safety reporting, and data integrity interview site personnel identify compliance gaps and assess overall site performance prepare and deliver a clear, risk-based audit report within agreed timelines communicate findings professionally with sponsor and site representatives requirements: proven experience conducting gcp investigator site audits (sponsor-side experience preferred) strong knowledge of ich-gcp and mexican clinical trial regulations fluent spanish and english preferred able to produce concise, high-quality audit reports available to conduct the audit on 6th–7th april this is a short-term contract opportunity with potential for future collaboration. If you are available and interested, please share your cv and confirm your availability.