Jobs in the Netherlands, in English.
39,000+ live jobsThis job is no longer available
This position has been filled or the listing has expired. Browse similar opportunities below.
Similar jobs still open
Quality & Compliance Manager
(Sr) Clinical Research Associate - Netherlands
Clinical Research Associate (Level I) - Netherlands, client dedicated
Manufacturing Compliance Coordinator
Regional Clinical Compliance Optimization Lead
Remote in the Netherlands·Full-time·Added 4 days ago
5 open roles
Our summary
- Salary
- €107,200 - €134,000 a year
- Work mode
- Remote (Netherlands)
- Contract
- Permanent, full-time hours
- Experience
- 10+ years




Skills
Requirements
What we're looking for
Bachelor's degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline* with 10+ years in clinical research, clinical operations, plus minimum 4 years *experience in a GCP compliance or equivalent role** (i.e. quality) is preferred
Nice to have
** Experience in data analytics, metrics and KPI management is preferred
Experience with RBQM principles, risk identification, and data-driven decision-making.
Experience in process improvement, operational excellence, or quality initiatives.
Experience supporting or implementing global process changes
Experience in oncology global trials is preferred.
Education & certifications
*Exceptions may be made for candidates with equivalent appropriate Clinical Operations experience.
Computer Skills: PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint)
Certification in quality management, clinical research, or process improvement methodologies (e.g., Lean Six Sigma) will be a plus
Pay & benefits
What you'll get
Salary Range Netherlands: 107,200.00 EUR - 134,000.00 EUR
The role
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
What you'll do
The Regional Clinical Compliance (RCC) Optimization Lead is responsible for proactively identifying signals, trends, and systemic issues across countries and EMEA region to drive continuous improvement in clinical trial execution and processes. This role plays a key part in translating operational insights into actionable improvements, partnering with Global Clinical Compliance, RBQM (Risk-Based Quality Management), and global process owners to enhance efficiency, compliance, and quality across the organization. Collaborates closely with RCC Inspection Lead and RCC Lead (including Country RCCs as needed).
Identify and analyze signals, trends, and systemic issues across EMEA using compliance-generated data, audit findings, inspection outcomes, and operational insights.
Translate aggregated insights into meaningful risk patterns and improvement opportunities.
Provide regular reporting and recommendations to stakeholders to support informed decision-making.
Propose and support process improvements based on identified trends and systemic issues.
Collaborate closely with RBQM teams to integrate findings into process risk assessment and risk mitigation strategies.
Ensure alignment of improvements with GCP requirements, company procedures, and quality standards
Identify areas of additional training and support for preparing and delivering such educational sessions within the EMEA region
Support regional and country-level process improvement initiatives to enhance efficiency, compliance, and consistency.
Act as a liaison between regional/country teams and Global Clinical Compliance and global process owners.
Facilitate the regional implementation of improvements identified at global, local or regional levels, ensuring scalability and sustainability.
Promote best practice sharing across countries and regions.
Partner cross-functionally with Clinical Operations, Quality Assurance, RBQM, and Global Compliance teams.
Influence stakeholders at multiple levels to drive the adoption of process enhancements.
Support change management activities related to new or updated processes.
Supervisory Responsibilities: Not applicable
About BeOne Medicines
- Founded
- 2010
- Employees
- 10,000+
- Headquarters
- Basel, Switzerland
In their own words
Additional information
Travel: up to 10% travel
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
- Fosters Teamwork
- Provides and Solicits Honest and Actionable Feedback
- Self-Awareness
- Acts Inclusively
- Demonstrates Initiative
- Entrepreneurial Mindset
- Continuous Learning
- Embraces Change
- Results-Oriented
- Analytical Thinking/Data Analysis
- Financial Excellence
- Communicates with Clarity
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.
