EMEA Clinical Compliance & Process Improvement Lead

BeOne Medicines Ltd.

Nederland

Ibrido

EUR 107.000 - 134.000

Tempo pieno

5 giorni fa
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Descrizione del lavoro

BeOne Medicines Ltd. seeks an experienced Regional Clinical Compliance Optimization Lead to drive signals-based improvements across the EMEA region.

You will translate operational insights into compliant, scalable processes and partner with Global Clinical Compliance and RBQM to optimize trial execution. You will collaborate with Clinical Operations, Quality Assurance and global process owners, supporting regional implementation and training efforts while traveling up to 10% to partner with

Competenze

  • Bachelor’s degree in a scientific, medical or healthcare discipline with 10+ years in clinical research and clinical operations, plus 4+ years in a GCP compliance or equivalent role.
  • Experience in data analytics, metrics and KPI management is preferred.
  • Experience with RBQM, risk identification and data-driven decision making is preferred.

Mansioni

  • Identify signals and trends across EMEA using compliance data, audit findings, and operational insights.
  • Translate insights into actionable improvements and work with Global Clinical Compliance and RBQM to enhance processes.
  • Lead regional and country-level process improvements for efficiency, compliance and consistency.
  • Collaborate with Clinical Operations, Quality Assurance and global teams; drive change management and adoption of new processes.
  • Travel up to 10% as needed.

Conoscenze

Signal detection
Trend analysis
Process improvement
Risk management
Operational excellence
Stakeholder collaboration
Change management
Data analytics
KPI management
RBQM

Formazione

Bachelor’s degree (BS/BA) in science/medical/healthcare

Strumenti

MS Office

Descrizione del lavoro

BeOne Medicines Ltd. seeks an experienced Regional Clinical Compliance Optimization Lead to drive signals-based improvements across the EMEA region.

You will translate operational insights into compliant, scalable processes and partner with Global Clinical Compliance and RBQM to optimize trial execution. You will collaborate with Clinical Operations, Quality Assurance and global process owners, supporting regional implementation and training efforts while traveling up to 10% to partner with

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