IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services, including consulting services. It has a network of more than 58,000 employees in more than 100 countries.As of 2017, IQVIA was reported to be one of the world's largest contract research organizations 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.