Clinical Research Manager

BeOne Medicines

. Act as line manager for trial monitoring staff (CRAs) in Belgium .

Posted 9/24/2026full-timeRemote • BelgiumMid-LevelSenior💰 €83,200 - €104,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical operations management, including trial monitoring, staff development, and adherence to ICH/GCP standards. Proficient in overseeing study start-up processes and ensuring compliance with local regulations while fostering team performance and operational excellence.

Highest-signal resume keywords

Clinical Operations ManagementTrial MonitoringICH/GCP ComplianceStaff DevelopmentOncology Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementPerformance AppraisalSite ActivationFeasibility AssessmentCAPA Development

Soft Skills

Interpersonal SkillsOrganizational SkillsLeadership Skills

Tools & Technologies

Microsoft WordMicrosoft ExcelMS ProjectMicrosoft PowerPointMicrosoft Outlook

Industry Keywords

BiotechPharmaceuticalCROClinical ResearchOncology

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Act as line manager for trial monitoring staff (CRAs) in Belgium
Plan, assign, and direct work; assess performance and guide professional development of direct reports
Participate in hiring selection and allocate resources to clinical research projects
Assign staff to clinical studies based on experience and training
Ensure clinical trial protocols are executed according to ICH/GCP, local regulations, and applicable SOPs
Collaborate with the Regional Clinical Operations Manager to maintain study timelines and quality standards
Support study start-up and provide local expertise
Manage study start-up and trial monitoring staff in accordance with company policies and regulations
Ensure onboarding and training of new employees and oversee training plans
Manage quality of assigned staff's clinical work through regular review and evaluation
Provide country-specific study start-up expertise and review study documents, drug labels, ICFs, and templates
Develop and review site-specific recruitment materials and tools
Collaborate with study teams and clinical sites on IRB/EC submissions, TMF completeness, site activation, enrollment, and inspection readiness
Contribute to feasibility, site identification, selection, and evaluation
Perform accompanied CRA visits and assess performance
Review visit reports, follow up on issue resolution, and communicate significant risks and proposed actions
Monitor workload and quality metrics through regular review and reporting
Anticipate and identify site issues, propose CAPAs, identify gaps, and leverage opportunities
Promote operating excellence and innovation
Contribute to Clinical Operations strategy and performance against key metrics
Mentor and manage junior staff and Clinical Research Associates
Act as escalation point for CRA site-related issues
Conduct mid-year and year-end performance appraisals for direct reports

Requirements

What you’ll need

Bachelor’s degree (or equivalent) or higher in a scientific, medical or healthcare discipline
Minimum 5-7 years progressive experience in clinical operations within the biotech/pharmaceutical sector
Prior clinical trial experience including experience in a management/leadership capacity
Experience in oncology is highly recommended
Ability to work independently and effectively handle multiple priorities in a fast-paced environment
Minimum 5-7 years progressive experience in clinical operations, preferably including at least 2 years of line management in the pharmaceutical or CRO industry
Excellent interpersonal skills and strong organizational skills
Fluent in German & the country language (writing and speaking)
Efficient in Microsoft Word, Excel, MS Project, MS PowerPoint and Outlook
Willingness to travel up to 30-40%