EMEA Clinical Compliance Optimization Lead

BeOne Medicines; Basel; Vor Ort; CHF 156.000 - 195.000; Vollzeit

Zusammenfassung

BeOne Medicines seeks an experienced Regional Clinical Compliance Optimization Lead to drive continuous improvement in clinical trial execution across the EMEA region. You will identify signals, trends, and systemic issues, translating insights into actionable improvements in collaboration with Global Clinical Compliance and RBQM teams.

The role requires a BA/BS in a scientific field, 10+ years in clinical research with at least 4 years in a GCP compliance or quality function, plus experience in

Qualifikationen

• Requires bachelor's in scientific/medical field with 10+ years in clinical research.
• Exceptions may be made for equivalent experience in Clinical Operations.
• Experience in data analytics, metrics and KPI management is preferred.

Aufgaben

• Identify signals, trends, and systemic issues across EMEA using compliance data, audit findings, inspection outcomes, and operational insights.
• Translate insights into meaningful risk patterns and improvement opportunities.
• Provide regular reporting and recommendations to stakeholders for informed decision-making.
• Propose and support process improvements based on identified trends and systemic issues.
• Collaborate with RBQM teams to integrate findings into process risk assessments and mitigation strategies.
• Ensure alignment of improvements with GCP requirements and quality standards.
• Identify training needs and support for regional education sessions.

Kenntnisse

RBQM principles

Data analytics

Process improvement

Quality management

Stakeholder management

Ausbildung

Bachelor’s degree in science/medical field

Tools

MS Office

Jobbeschreibung

BeOne Medicines seeks an experienced Regional Clinical Compliance Optimization Lead to drive continuous improvement in clinical trial execution across the EMEA region. You will identify signals, trends, and systemic issues, translating insights into actionable improvements in collaboration with Global Clinical Compliance and RBQM teams.

The role requires a BA/BS in a scientific field, 10+ years in clinical research with at least 4 years in a GCP compliance or quality function, plus experience in