Compliance Clinical Trials Assistant

Responsibilities

• Perform document oversight by managing and organizing essential trial documents, such as the Trial Master File (TMF).
• Provide regulatory compliance support to ensure studies adhere to GCP, SOPs, and other regulatory requirements.
• Support audit and inspection readiness for regulatory bodies like the MHRA and FDA.
• Monitor and report on compliance metrics, deviations, and quality issues.
• Identify process gaps and contribute to the improvement of compliance workflows.

Requirements

• Previous compliance experience within clinical trials is required.
• Strong knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• A degree in life sciences or equivalent industry experience.
• Fluency in English.
• Must hold valid right to work for the country of residence (visa sponsorship is not available).

About the Company

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.