Senior GCP Compliance & Audit Specialist

MMS; Manchester; On-site; GBP 65,000 - 90,000; Full time

Job summary

MMS in Manchester is seeking an experienced GCP Auditor to safeguard trial data integrity and regulatory compliance across UK/EU audits. You will plan, conduct, and document audits of clinical sites and vendors, ensuring adherence to 21 CFR Part 11, FDA, and GxP requirements.

Join a data-focused CRO recognized for a great culture and collaborative teams. Travel up to 30% within the UK/EU, and contribute to CAPA resolutions and process improvements while working with multidisciplinary colleagues.

Qualifications

• Must have regulatory and GCP knowledge with clinical trial exposure.
• Minimum 5 years’ experience in GCP regulated industry.
• Willing to travel up to 30% within the UK/EU.

Skills

Regulatory updates

GCP audits

Audit docs

CAPA planning

Vendor monitoring

Communication

Education

Science/medical degree

Masters preferred

Tools

MS Office

Job description

MMS in Manchester is seeking an experienced GCP Auditor to safeguard trial data integrity and regulatory compliance across UK/EU audits. You will plan, conduct, and document audits of clinical sites and vendors, ensuring adherence to 21 CFR Part 11, FDA, and GxP requirements.

Join a data-focused CRO recognized for a great culture and collaborative teams. Travel up to 30% within the UK/EU, and contribute to CAPA resolutions and process improvements while working with multidisciplinary colleagues.