EMEA Clinical Compliance & Process Optimization Lead

BeOne Medicines USA; Paesi Bassi; In loco; EUR 107.000 - 134.000; Tempo pieno

Descrizione del lavoro

BeOne Medicines USA seeks an Regional Clinical Compliance Optimization Lead to identify signals, trends, and systemic issues across the EMEA region, driving continuous improvement in trial execution and processes. You will collaborate with Global Clinical Compliance, RBQM, and process owners to enhance efficiency, quality, and compliance, working with RCCs and country teams as needed.

Travel up to 10% is expected; a BS/BA or higher in a scientific field with 10+ years in clinical research and at

Competenze

• 10+ years in clinical research or clinical operations with GCP/compliance experience.
• Experience in data analytics, metrics and KPI management is preferred.
• RBQM principles and data-driven decision making.
• Certification in quality management or clinical research is a plus.
• Experience supporting or implementing global process changes; travel up to 10%.

Mansioni

• Identify signals, trends, and systemic issues across the EMEA region to drive continuous improvement in trial execution and processes.
• Collaborate with RBQM teams to integrate findings into process risk assessment and mitigation.
• Translate insights into actionable recommendations for stakeholders and drive regional implementation of improvements.
• Act as liaison between regional teams and Global Clinical Compliance and process owners; promote best practice sharing.
• Support change management activities related to new or updated processes.

Conoscenze

Data analytics

Metrics management

KPI management

RBQM principles

Process improvement

Quality initiatives

GCP compliance

Clinical operations

Stakeholder collaboration

Change management

Formazione

Bachelor's degree in scientific/medical/healthcare

Strumenti

MS Office

Descrizione del lavoro

BeOne Medicines USA seeks an Regional Clinical Compliance Optimization Lead to identify signals, trends, and systemic issues across the EMEA region, driving continuous improvement in trial execution and processes. You will collaborate with Global Clinical Compliance, RBQM, and process owners to enhance efficiency, quality, and compliance, working with RCCs and country teams as needed.

Travel up to 10% is expected; a BS/BA or higher in a scientific field with 10+ years in clinical research and at