Compliance Clinical Trials Assistant – Clinical Research

About the role

IQVIA is looking for a Compliance Clinical Trials Assistant to support its sponsor‑dedicated team across EMEA. The role focuses on ensuring trial documentation and processes meet regulatory standards and quality expectations.

Key responsibilities

• Manage and organise essential trial documents, including the Trial Master File (TMF).
• Support regulatory compliance by applying GCP, SOPs, and other relevant guidelines.
• Assist in audit and inspection readiness for regulators such as MHRA and FDA.
• Track and report compliance metrics, deviations, and quality issues.
• Identify gaps and contribute to process‑improvement initiatives.

Required profile

• Previous compliance experience within clinical trials.
• Fluent in English.
• Knowledge of Good Clinical Practice (GCP) and ICH guidelines.
• Degree in life sciences or equivalent industry experience.
• Valid right to work in the country of residence (no visa sponsorship).

Required skills

• Good Clinical Practice (GCP)
• International Conference on Harmonisation (ICH) regulations
• Trial Master File (TMF) management