Compliance Clinical Trials Assistant – Regulatory Support

About the role

IQVIA is seeking a Compliance Clinical Trials Assistant to support its sponsor‑dedicated team across EMEA. The role focuses on ensuring that clinical studies adhere to regulatory standards and internal quality processes.

Key responsibilities

• Document oversight – manage and organise essential trial documents such as 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 by regulators (e.g., MHRA, FDA).
• Tracking and reporting – monitor compliance metrics, deviations and quality issues.
• Process improvement – identify gaps and help enhance compliance processes.

Required profile

• Previous compliance experience within clinical trials.
• Fluent English communication.
• 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) knowledge.
• International Conference on Harmonisation (ICH) knowledge.

What we offer

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