Regional Clinical Compliance Inspection Manager
Spain·€69,600 - €87,000·On-site·Mid · 5+ years·Permanent·English: Required
Need a visa?Salary meets the Highly Qualified Professional (PAC) threshold; employer support is not confirmed — this job may fit the Highly qualified / Blue Card route.
About the role
TheRegionalClinical Compliance(RCC)InspectionManageris responsible fordriving proactive risk management, sustained inspection readiness, audit support, and regulatory compliance across clinical trials. The role provides leadership and oversight to ensure consistent implementation of GCP and regulatory requirements, effectiveinspectionreadiness programs, and successful management of inspections and audits.
Key responsibilities include leading inspection readiness and audit support activities at regional or global levels, guiding clinical teams on inspection expectations, coordinating audit and inspection responses, and ensuringtimely, high-quality, and compliant remediation. The role also drives a proactiveinspection/auditreadiness culture,to effectively manage complex, high-risk inspections whilemaintainingcontinuous readiness.
What you'll do
Organize briefing materials,logistics, and stakeholder alignment
Supportinspection readiness across the EMEA region
Supportimplementation of standards, tools, and best practices
Ensure teams are inspection-ready through training and guidance
Assess inspection risks and oversee mitigation plans
Supportsmock inspections and readiness assessments
Maintain inspection-ready documentation, processes, and systems
Supports development ofstory boards based on global story boards templates and structure and acting as subject matter expert (SME) in content generationtogether with therelevant functional area SMEs
Supportregionalpreparation activities for regulatory inspections and internal/external audits
Coordinate cross-functional stakeholders (Clinical Operations, QA, country teams)
Align withRegional Clinical ComplianceLeadto conduct targeted site preparation visitsasrequired
Lead and coordinate responses to inspection/audit findings
Manage CAPAs, including risk assessment, root cause analysis, and effectiveness checks
Track CAPAs totimelyand effective closure
Ensure robust root cause analysis and sustainable corrective actions
Oversee CAPA strategies and regulatory commitments
Drive consistent, high-quality organizational responses
Monitor trends andidentifyopportunities for continuous improvement
What we're looking for
Understanding of clinical trial processes with a thorough knowledge of ICH-GCP and associated regulatoryguidelines
Analytical andproblem-solvingskillsand high attention to detail,and quality orientation
Excellent communication and stakeholder management skills
Influence senior stakeholders and decision-making
Excellent English written and verbal communication andinterpersonal skills
Excellent organizational skills and ability to prioritize and multi-task
Ability to work independently in multi-cultural setting and effectively handle multiple priorities in a fast-paced environment
Not applicable
Bachelor's degree (BS/BA or equivalent) or higher in a scientific,medicalor healthcare discipline* with 5+ years in clinical research, clinical operations, or compliance
Computer Skills:PC literacyrequired; MSOffice skills (Outlook, Word, Excel, PowerPoint)
Experience inCAPA development and tracking
Experienceininspections and auditsmanagement,including mock inspectionsandmock interviews
Deep knowledge ofICH-GCP, regulatory requirementsandClinical trial processes end-to-end
Nice to have
Minimum 4years'**experience in a GCP compliance or equivalent role*(i.e. quality) is preferred.
*exceptionsmay be made for candidates with equivalentappropriate ClinicalOperations experience.
** Experience in management of inspections and audits is preferred
Experience in oncology global trials is preferred
What you'll get
Salary Range Spain: 69,600.00 EUR - 87,000.00 EUR
How you'll work
Travel:upto15-20% travel
About the company & team
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.
Additional information
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.
About the company
BeOne Medicines
Company