Proflie: Work as a GCP QA auditor and clinical research monitor since 2019. Experienced in doing global ICH-GCP audits for pharma companies & CROs. Clinical monitoring experience in the start-up, monitoring and close out of Phase I-IV clinical studies. Perform site specific and clinical trial specific audits on Pharma and CROs. Perform General Qualification audits. Execution of audit to full report writing and review audit responses by auditees. Experience in phase I-IV clinical trials in a range of therapeutic areas. Expert in medical writing. Can audit in any European country. Have also performed remote audits in Australia and the USA .Experience in Australia, Japan, Europe and the US. Language Expertise: fluent English and conversational French and Italian. Current City: London.