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Senior Clinical Research Associate - Job Opportunity at IQVIA

Remote, Netherlands
Full-time
Senior
Posted: April 26, 2025
Remote
EUR 65,000 - 85,000 annually based on Dutch market conditions and senior level position

Benefits

Comprehensive professional development programs
Advanced clinical research technology access
Therapeutic specialization opportunities
Global project exposure

Key Responsibilities

Lead site monitoring and quality assurance across clinical trial phases
Drive subject recruitment strategy and optimization
Manage protocol compliance and regulatory adherence
Oversee site documentation and regulatory submissions
Direct communication with research sites and stakeholders
Ensure data integrity and GCP compliance

Requirements

Education

Bachelor's Degree or Master's Degree in scientific discipline or healthcare

Experience

Minimum of 12 months of independent monitoring experience

Required Skills

Good Clinical Practice (GCP) knowledge ICH guidelines expertise Written and verbal communication skills English and Dutch language fluency Site monitoring expertise Clinical trial documentation management Regulatory compliance understanding

Certifications

GCP certification (implied)
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Industry Trends

Increasing adoption of decentralized clinical trials is reshaping monitoring approaches and requiring enhanced technical competencies Growing focus on real-world evidence integration is expanding the traditional CRA role Rising demand for therapeutic area specialization as trials become more complex Shift towards risk-based monitoring requiring advanced analytical skills

Role Significance

Typically works within a matrix team of 5-8 professionals including project managers and data specialists
Senior position with significant autonomy in trial management and site oversight

Key Projects

Phase II-IV clinical trials in multiple therapeutic areas Complex multi-site international studies Protocol optimization initiatives Site performance improvement programs

Success Factors

Strong therapeutic area expertise combined with broad clinical research knowledge Excellent stakeholder management across multiple cultural contexts Ability to balance quality requirements with operational efficiency Proactive risk identification and mitigation capabilities

Market Demand

High demand with sustained growth projected due to increasing clinical trial complexity and volume in EU markets

Important Skills

Critical Skills

GCP/ICH expertise - essential for ensuring trial compliance and quality Communication skills - crucial for site management and stakeholder coordination Technical proficiency - required for modern clinical trial management systems Therapeutic area knowledge - vital for protocol understanding and site support

Beneficial Skills

Project management capabilities Data analytics understanding Risk-based monitoring experience Change management skills

Unique Aspects

Access to proprietary CRA-developed technology platforms
Therapeutic area specialization opportunities
Global project exposure with local support structure
Strong emphasis on professional development and career advancement

Career Growth

2-4 years in role typically required before advancement to management positions

Potential Next Roles

Clinical Research Manager Project Manager Clinical Operations Director Regional Monitoring Manager

Company Overview

IQVIA

IQVIA stands as a global leader in clinical research and healthcare intelligence, formed through the strategic merger of IMS Health and Quintiles

Industry leader with significant market share in clinical research services and healthcare analytics
Strong European presence with established Netherlands operations supporting global clinical trials
Professional environment emphasizing diversity, innovation, and continuous learning with strong focus on work-life balance
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