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.