Compliance Clinical Trials Assistant

Job description

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: Please note: This role is not eligible for visa sponsorship and candidates must hold valid right to work for country of residence. Apply today and forge a career with greater purpose, make an impact, and never stop learning! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create int...