Requirements

• 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.

• 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