We are seeking an experienced Compliance Clinical Trials Assistant to join our cFSP (sponsor-dedicated) team in EMEA.

Candidates are required to have previous compliance experience within clinical trials to be considered.

Key Responsibilities

• Document oversight - managing and organising essential trial documents (e.g., Trial Master File / TMF)
• Regulatory compliance support - ensuring studies follow guidelines like GCP (Good Clinical Practice), SOPs, and regulatory requirements
• Audit and inspection readiness - supporting preparation for audits or inspections from regulators (e.g., MHRA, FDA)
• Tracking and reporting - monitoring compliance metrics, deviations, and quality issues
• Process improvement - identifying gaps and helping improve compliance processes

What We’re Looking For

• Previous compliance experience within clinical trials required.
• Cand...