Compliance Clinical Trials Assistant

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. Candidate must speak English Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH). Degree in life sciences or equivalent industry experience. Please note: This role is not eligible for visa sponsorship and candidates must hold valid right to work for country of residence.