Compliance Clinical Trials Assistant

About the role

IQVIA is looking for a Compliance Clinical Trials Assistant to join its sponsor‑dedicated cFSP team serving the EMEA region. The role supports the preparation and maintenance of trial documentation, ensures regulatory compliance, and helps the team stay audit‑ready.

Key responsibilities

• Document oversight – manage and organise essential trial documents, including the Trial Master File (TMF).
• Regulatory compliance support – ensure studies follow GCP, SOPs and other regulatory requirements.
• Audit and inspection readiness – assist in preparing for audits or inspections from regulators such as MHRA and FDA.
• Tracking and reporting – monitor compliance metrics, deviations and quality issues.
• Process improvement – identify gaps and contribute to enhancing compliance processes.

Required profile

• Previous compliance experience within clinical trials.
• Fluent English communication.
• 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

What we offer

• Opportunity to work with a global leader in clinical research services.
• Career development in a purpose‑driven environment.