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Clinical Research Associate with French - Job Opportunity at Boston Scientific Corporation

Kerkrade, Netherlands
Full-time
Mid-level
Posted: March 14, 2025
Hybrid
EUR 45,000 - 65,000 annually based on EMEA market rates for mid-level CRAs with language skills

Benefits

Comprehensive hybrid work arrangement with flexible scheduling to support work-life integration
Professional development through upskilling programs and mentorship opportunities
Competitive benefits package aligned with multinational medical device industry standards
Career advancement opportunities within a global healthcare leader
Stable employment with a Fortune 500 medical technology company

Key Responsibilities

Lead multi-site regulatory submissions and essential document management across EMEA region, directly impacting clinical trial timelines and compliance
Drive strategic partnerships with clinical research sites through informed consent form negotiations and customization
Orchestrate cross-functional collaboration to achieve clinical research objectives and maintain quality standards
Manage complex documentation processes across multiple concurrent clinical trials
Ensure regulatory compliance with ICH/GCP, MDR, and GDPR requirements while maintaining study integrity
Develop and execute site readiness strategies across multiple research locations
Provide strategic oversight of site start-up activities and maintain critical study metrics

Requirements

Education

Degree in a relevant scientific or healthcare subject

Experience

2/5 years of experience in study submissions to Ethics Committees in France

Required Skills

Fluency in French and English Strong communication skills Problem-solving capabilities Learning agility Independent work capability Team collaboration
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Sauge AI Market Intelligence

Industry Trends

Increasing focus on decentralized clinical trials and remote monitoring capabilities is reshaping CRA roles Growing demand for multilingual clinical research professionals in the EMEA region due to cross-border trial expansion Rising importance of data privacy and GDPR compliance expertise in clinical research Shift towards integrated clinical trial management systems and eTMF solutions requiring enhanced technical proficiency

Role Significance

Typically part of a 5-10 person clinical operations team with matrix reporting to regional and global clinical leads
Mid-level position with significant autonomy in site management and regulatory compliance

Key Projects

Multi-site clinical trial coordination across EMEA region Regulatory submission management for novel medical device studies Site relationship development and management programs Quality assurance and compliance initiatives

Success Factors

Strong understanding of European regulatory landscape and EC submission requirements Excellent stakeholder management skills across multiple cultures and languages Ability to balance multiple concurrent studies while maintaining quality standards Proactive problem-solving approach to site start-up challenges

Market Demand

High demand with significant growth potential due to expanding clinical trial activities in Europe and increasing regulatory complexity

Important Skills

Critical Skills

French language proficiency essential for EC submissions and site communication Regulatory knowledge specific to French and Belgian clinical research environment Clinical trial documentation management expertise Strong project coordination capabilities

Beneficial Skills

Additional European language skills Experience with electronic trial master file systems Knowledge of medical device regulations Change management capabilities

Unique Aspects

Opportunity to work with cutting-edge medical devices in a multinational setting
Strong focus on language skills and cross-cultural communication
Balance of independent work and team collaboration in a hybrid environment
Exposure to multiple therapeutic areas and research methodologies

Career Growth

2-3 years in role before advancement opportunity, with accelerated progression possible based on performance and business needs

Potential Next Roles

Senior Clinical Research Associate Clinical Project Manager Regional Clinical Operations Lead Clinical Research Manager

Company Overview

Boston Scientific Corporation

Boston Scientific is a leading global medical technology company with a strong focus on innovative medical solutions and clinical research

Top-tier medical device manufacturer with significant market presence and consistent growth trajectory
Strategic EMEA hub position indicating strong regional investment and growth potential
Professional environment with emphasis on innovation, diversity, and global collaboration
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