Key Skills

Job Description

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. General Description 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). Essential Functions Of The Job Signal Detection & Trend Analysis 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. Process Improvement & Risk Management 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 Operational Excellence & Implementation 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. Stakeholder Collaboration & Influence 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 Education Required 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 Exceptions may be made for candidates with equivalent appropriate Clinical Operations experience. Experience in data analytics, metrics and KPI management is preferred Computer Skills: PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint) Other Qualifications Experience with RBQM principles, risk identification, and data-driven decision-making. Experience in process improvement, operational excellence, or quality initiatives. Certification in quality management, clinical research, or process improvement methodologies (e.g., Lean Six Sigma) will be a plus Experience supporting or implementing global process changes Experience in oncology global trials is preferred. Travel: up to 10% travel Salary Range Netherlands: 107,200.00 EUR - 134,000.00 EUR 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.

Core Responsibilities

Identify and analyze compliance signals, trends, and systemic issues across EMEA, translating findings into risk patterns, recommendations, and process improvements. Partner with regional and global teams to implement sustainable improvements, support risk mitigation and change management, and promote consistent clinical trial execution.

Requirements

A bachelor’s degree or higher in a scientific, medical, or healthcare discipline and more than 10 years of clinical research or clinical operations experience are required, including at least four years in GCP compliance or an equivalent quality role preferred; equivalent clinical operations experience may be considered. Experience with RBQM, data-driven decision-making, process improvement, global process changes, and oncology trials is valued, while data analytics and KPI management experience is preferred.