Regional Clinical Compliance Manager

BeOne Medicines

Regional Clinical Compliance Country Manager overseeing clinical trial compliance in Spain. Engaging stakeholders while ensuring adherence to Good Clinical Practice and regulatory requirements.

Posted 7/17/2026full-timeRemote • 🇪🇸 SpainMid-LevelSenior💰 €69,600 - €87,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial compliance, with a strong understanding of ICH-GCP guidelines and the ability to manage compliance risks effectively. Proficient in conducting site compliance visits and supporting corrective and preventive actions (CAPAs) while ensuring high-quality standards.

Highest-signal resume keywords

GCP ComplianceClinical Trial ProcessesRisk ManagementAnalytical SkillsBilingual Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical OperationsCompliance OversightRisk EvaluationSite Compliance VisitsCorrective and Preventive Actions

Soft Skills

Attention to DetailProblem-SolvingOrganizational SkillsInterpersonal SkillsMultitasking

Tools & Technologies

MS OfficeOutlookWordExcelPowerPoint

Industry Keywords

ICH-GCPClinical TrialsRegulatory GuidelinesHealthcare DisciplineScientific Degree

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Ensure robust oversight of clinical trial compliance at the country and site level
Apply a risk-based approach to proactively identify, evaluate, and manage compliance risks
Serve as the primary point of contact for country teams regarding GCP requirements and company procedures
Analyze and confirm initial country and site-specific risks and identify high-risk sites
Conduct Site Compliance Visits on identified high-risk sites
Support country teams in identifying, managing, and resolving compliance issues
Support and manage individual Corrective and Preventive Actions (CAPAs)

Requirements

What you’ll need

Bachelor’s degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline
Minimum of 5 years of progressive experience in clinical operations roles
Minimum 4 years’ experience in a GCP compliance or equivalent role
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 English and Spanish written and verbal communication and interpersonal skills
Excellent organizational skills and ability to prioritize and multitask
PC literacy required; MSOffice skills (Outlook, Word, Excel, PowerPoint)

Benefits

Comp & perks

Health insurance
Retirement plans
Paid time off
Flexible work arrangements
Professional development opportunities