Senior Clinical Research Associate, French, Dutch Fluency

Alimentiv

Lead CRA overseeing monitoring, recruitment and site management for Alimentiv’s multinational clinical trials in Belgium. Serving as primary liaison among sites, CRAs and project teams while ensuring GCP compliance.

Posted 8/7/2026full-timeRemote • 🇧🇪 BelgiumSenior💰 €58,000 - €78,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical site monitoring, project management, and regulatory compliance, with a strong focus on GCP best practices and effective stakeholder communication. Proficient in training and mentoring CRAs while optimizing patient recruitment and site management.

Highest-signal resume keywords

Clinical Site MonitoringGCP Best PracticesProject ManagementStakeholder CommunicationFluency in English, Dutch, and French

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Site ManagementProject Monitoring ServicesSOP KnowledgeData ManagementBudget MonitoringProtocol DevelopmentCRF DevelopmentSite Investigator RecruitmentPatient Recruitment OptimizationRegulatory Filing Management

Soft Skills

Strong Communication SkillsSelf-MotivationAttention to DetailCritical ThinkingRelationship Building

Industry Keywords

Clinical ResearchCRA TrainingStudy GuidelinesSite Access ComplianceTrial Materials Coordination

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Manage, deliver and/or perform full clinical site monitoring services for one or more projects
Design and oversee project monitoring services, including training, site/patient recruitment, site data/document management, monitoring project site budgets and regulatory filings
Ensure activities align with SOPs, study guidelines and GCP best practices
Act as primary liaison between CRAs and the project team as Lead CRA
Participate in developing project plans, protocols, CRFs, communications, monitoring forms, documents and tools
Maintain collaborative relationships with stakeholders
Act as subject matter expert, mentor, coach and provide performance feedback for peers
Assist with CRA selection, hiring, training and supervision; perform co-monitoring and training visits
Serve as escalation point for site/patient issues and Sponsor concerns
Identify and recruit site investigators and coordinate delivery of trial materials and documents
Optimize patient recruitment and provide guidance on inclusion/exclusion criteria
Serve as primary clinical site contact and oversee study integrity
Support site access to study systems and compliance with project-specific training
Follow site-related issues through resolution
Coordinate clinical-site communications with project teams throughout the project lifecycle

Requirements

What you’ll need

Minimum of a college diploma/degree
4–6 years of related experience
Strong communication skills
Self-motivation and commitment to achieving positive results
Strong attention to detail
Ability to build collaborative relationships
Critical thinking abilities
Ability to regularly travel to clinical sites
Must be fluent in English, Dutch and French
Knowledge and application of SOPs, study guidelines and GCP best practices

Benefits

Comp & perks

One-time sign-on bonus of €3,000
Annual Bonus (Short Term Incentive Program) target of 8% of annual salary
Monthly stipend of €157.83 to offset business communication costs
Monthly cell phone stipend of €40
One-time expense reimbursement of up to €500 for office items
Mileage reimbursement for travel