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