Regional Clinical Compliance Optimization Lead

BeiGene · Basel, Switzerland · Onsite · CHF156,200 - CHF195,200/year
Listed via Workday
Posted Jul 17, 2026 · Apply by Sep 16
Recently checked

Last checked active on Jul 18, 2026.

Position Overview

Compensation: CHF156,200 - CHF195,200/year
Position: Mid
Type: Job
Employment: Full time
Practice Area: Compliance
Remote: No
Deadline: Sep 16, 2026

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 Switzerland: 156,200.00 CHF - 195,200.00 CHF

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.

Compensation

CHF156,200 - CHF195,200/year

Practice Area

Position

Mid

Industry

Legal

Application Deadline

September 16, 2026

Employment Type

Full time

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