IQVIA is seeking an experienced Compliance Clinical Trials Assistant to join our cFSP (sponsor-dedicated) team in EMEA. This role involves managing essential trial documents, ensuring compliance with GCP and regulatory guidelines, and preparing for audits.

Candidates must have previous compliance experience within clinical trials and a degree in life sciences. Fluency in English is required. Please note that visa sponsorship is not available, and candidates must have the right to work in Spain.