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.

Apply

RemoteFull-timeEntry LevelGCP

Salary

Not specified

Work Location

Leiden, South Holland, Netherlands, NL

Work Model

Remote

Employment Type

Full-time

Experience Level

Not Applicable

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