Regional Clinical Compliance Manager

General Description

Regional Clinical Compliance Country Manager is responsible for ensuring robust oversight of clinical trial compliance at the country and site level. This role applies a risk‑based approach to proactively identify, evaluate, and manage compliance risks, ensuring adherence to Good Clinical Practice (GCP), company procedures, and regulatory requirements. The role partners closely with country, regional and global stakeholders to safeguard patient safety, data integrity, and inspection readiness.

Essential Functions of the Job

Compliance Subject Matter Expert

• Serve as the primary point of contact for country teams regarding: GCP requirements, Company and study‑specific procedures, General compliance‑related queries
• Provide expert guidance and interpretation of regulations and internal standards to ensure consistent and compliant practices

Risk‑Based Country and Site Oversight

• Analyze and confirm initial country and site‑specific risks, including identification of critical data and key processes
• Communicate identified country and site trends, lessons learned with Clinical Operations functions for continuous improvement of study conduct compliance
• Align with Global Clinical Compliance on the execution of the Study Health Check Plan at country and site level
• Lead and support key process reviews through remote desk checks, ensuring alignment with Clinical Research Associate, Clinical Study Managers (CSMs) and respective Line Managers
• Identify high‑risk sites using a structured, risk‑based approach, including but not limited to: Historical performance and inspection outcomes, Planned and actual recruitment volumes, Feasibility assessments and risks identified during site selection and qualification, Non‑compliances identified during the study conduct
• Conduct Site Compliance Visits on identified high‑risk sites on a risk‑based approach

Issue Management & Audit and Inspection Support

• Support country teams in identifying, managing, and resolving compliance issues
• Support and manage individual Corrective and Preventive Actions (CAPAs) to ensure issues/deviations are thoroughly evaluated (including a risk assessment, root cause analysis and effectiveness measures) and identified actions are addressed in a timely manner
• As needed, support the Regional Clinical Compliance Inspection and Audit Support team, providing input to enable the preparation and conduct of the site audits and inspections

Core Competencies, Knowledge and Skill Requirements

• Understanding of clinical trial processes with a thorough knowledge of ICH‑GCP and associated regulatory guidelines
• Analytical and problem‑solving skills
• High attention to detail and quality orientation
• Excellent communication and stakeholder management skills

Communication & Interpersonal Skills

• Excellent English and French written and verbal communication and interpersonal skills
• Excellent organizational skills and ability to prioritize and multitask
• Ability to work independently in a multi‑cultural setting and effectively handle multiple priorities in a fast‑paced environment

Education Required

Bachelor’s degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline with a minimum of 5 years of progressive experience in clinical operations roles plus minimum 4 years’ experience in a GCP compliance or equivalent role (i.e., quality) is preferred. Experience in oncology global trials is preferred. Exceptions may be made for candidates with equivalent appropriate Clinical Operations experience.

Supervisory Responsibilities

Not applicable

Computer Skills

PC literacy required; MSOffice skills (Outlook, Word, Excel, PowerPoint)

Other Qualifications

Not applicable

Travel

Up to 20-30% travel

Salary Range EU

65,800.00 EUR - 82,200.00 EUR

Global Competencies

• 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

Equal Opportunity Statement

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.