Leiden
27 May 2026
Compliance Clinical Trials Assistant
IQVIA
Leiden
27 May 2026
Compliance Clinical Trials Assistant
We are seeking an experienced Compliance Clinical Trials Assistant to join our cFSP (sponsor-dedicated) team in EMEA. Candidates require previous compliance experience within clinical trials. This remote role involves document oversight, regulatory compliance support, and audit readiness.
RemoteFull-timeEntry LevelGCPICH
Compliance Clinical Trials Assistant
We are seeking an experienced Compliance Clinical Trials Assistant to join our cFSP (sponsor-dedicated) team in EMEA. Candidates require previous compliance experience within clinical trials. This remote role involves document oversight, regulatory compliance support, and audit readiness.
RemoteFull-timeEntry LevelGCP
Salary
Not specified
Core Qualifications
Technical (Must-have)
GCPICHTrial Master Fileregulatory compliance
Key Responsibilities
- Document oversight - managing and organising essential trial documents (e.g., Trial Master File / TMF)
- Regulatory compliance support - ensuring studies follow guidelines like GCP, SOPs, and regulatory requirements
- Audit and inspection readiness - supporting preparation for audits or inspections from regulators (e.g., MHRA, FDA)
- Tracking and reporting - monitoring compliance metrics, deviations, and quality issues
- Process improvement - identifying gaps and helping improve compliance processes
ComplianceClinical TrialsGCPICHTMFAuditRemoteEMEAIQVIAHealthcare