Clinical Research Associate, Belgium, Netherlands

Allucent

Clinical Research Associate overseeing monitoring for clinical trials at Allucent, ensuring compliance with regulations and protocols. Building site relationships and managing trial integrity through collaborative efforts.

Posted 7/21/2026full-timeAmsterdam • 🇳🇱 NetherlandsJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trial monitoring activities, ensuring compliance with ICH-GCP and regulatory guidelines while fostering strong site relationships. Proficient in identifying and resolving site issues to maintain trial integrity and patient safety.

Highest-signal resume keywords

Clinical Trial MonitoringICH-GCP ComplianceRegulatory AffairsBilingual Communication (English and German)Site Relationship Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementMonitoring ActivitiesData CollectionRegulatory ComplianceSite ActivationStudy StartupIssue ResolutionProtocol AdherenceGCP KnowledgeSOP Familiarity

Soft Skills

Clear CommunicationIndependent WorkPriority Management

Industry Keywords

Clinical TrialsGCPICHSOPsRegulatory RequirementsPatient SafetySite InitiationClose-Out VisitsTrial IntegrityMonitoring Phases

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection.
Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
Activities around regulatory affairs, site activation and study-startup.

Requirements

What you’ll need

Experience in leading monitoring activities in complex trials with a minimum of 2 years’ experience.
Strong understanding of ICH-GCP and regulatory guidelines.
Clear and confident communicator in English and German.
Comfortable working independently and managing priorities.
Willingness to travel, as required (8 DOS per month).

Benefits

Comp & perks

Comprehensive benefits package per location
Competitive salaries per location
Departmental Study/Training Budget for furthering professional development
Flexible Working hours (within reason)
Opportunity for remote/office-based* working depending on location
Leadership and mentoring opportunities
Participation in our enriching Buddy Program as a new or existing employee
Internal growth opportunities and career progression
Financially rewarding internal employee referral program
Access to online soft-skills and technical training via GoodHabitz and internal platforms
Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees