Clinical Project Specialist
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• Current
Location:
Brussels, Belgium Relevant
Experience:
5+ YearsProfessional Summary: Experienced Clinical Project Specialist with over 5 years of experience supporting global clinical and medical device studies. Strong background in subject selection committee workflows, adjudication activities, vendor and stakeholder coordination, data tracking, documentation management, database maintenance, and ensuring compliance with GCP and regulatory requirements. Key Skills & Expertise:
• Committee management and adjudication processes
• Clinical study coordination and operations support
• Vendor, site, and stakeholder management
• Clinical data tracking and review management
• Study documentation and database maintenance
• GCP compliance and regulatory adherence
• Cross-functional collaboration with study teams and core laboratories
• Clinical project coordination and execution Tools & Technologies:
• Clinical Trial Management Applications
• Microsoft Office Suite
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