Compliance Clinical Trials Assistant (EMEA)

About the role

We are looking for an experienced Compliance Clinical Trials Assistant to support our sponsor‑dedicated cFSP team across the EMEA region. The role ensures that clinical studies adhere to regulatory standards and internal quality processes.

Key responsibilities

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

Required profile

• Previous compliance experience within clinical trials.
• Fluent English communication.
• Knowledge of GCP, ICH and other clinical research regulatory requirements.
• Degree in life sciences or equivalent industry experience.
• Valid right to work in the country of residence (no visa sponsorship).

Required skills