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Site Monitor II - Job Opportunity at Parexel

Amsterdam, Netherlands
Full-time
Mid-level
Posted: April 10, 2025
Hybrid
EUR 45,000 - 65,000 annually based on Amsterdam market rates for clinical research professionals

Benefits

Remote work flexibility
Career development opportunities in clinical research
Global exposure in pharmaceutical industry
Professional training and development

Key Responsibilities

Ensure regulatory compliance and ICH-GCP protocol adherence through comprehensive site monitoring
Evaluate site performance and develop strategic action plans
Conduct both remote and on-site monitoring activities
Manage source document verification and clinical data accuracy
Coordinate with project teams for issue escalation and resolution
Document and track monitoring activities and protocol deviations

Requirements

Education

Bachelor's degree or Registered Nurse (RN) in a related field

Experience

Minimum of 1 year experience as a clinical monitor

Required Skills

ICH/GCP Guidelines knowledge Clinical trial monitoring experience CTMS system proficiency Fluent Dutch and English language skills Strong communication and relationship building Computer proficiency Adaptability to new technologies
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Industry Trends

Increasing adoption of decentralized clinical trials is reshaping monitoring roles Growing demand for hybrid monitoring capabilities combining remote and on-site skills Rising importance of technology proficiency in clinical research operations Expanding European clinical trial market creating sustained demand for experienced monitors

Role Significance

Typically works within a team of 5-8 monitors under a clinical research manager
Mid-level position with significant responsibility for trial quality and compliance

Key Projects

Phase II-IV clinical trials oversight Site performance optimization initiatives Protocol compliance management Data quality assurance programs

Success Factors

Strong understanding of clinical research regulations and practices Excellent balance of technical knowledge and interpersonal skills Ability to work independently while maintaining team collaboration Effective time management for both remote and on-site activities

Market Demand

High demand driven by expanding clinical trial activities in the Netherlands and broader EU region

Important Skills

Critical Skills

ICH-GCP knowledge for ensuring trial compliance and quality Bilingual proficiency for effective site communication Technical adaptability for evolving monitoring systems Strong documentation and reporting capabilities

Beneficial Skills

Experience with decentralized trial methodologies Knowledge of additional European languages Project management skills Understanding of risk-based monitoring approaches

Unique Aspects

Hybrid monitoring model combining remote and on-site activities
Strong focus on technological adaptation and system proficiency
Bilingual requirement reflecting important regional market position

Career Growth

2-3 years in role before advancement opportunity, depending on performance and project complexity

Potential Next Roles

Senior Clinical Research Associate Clinical Trial Manager Clinical Operations Manager Regional Monitoring Manager

Company Overview

Parexel

Parexel is a leading global clinical research organization (CRO) providing comprehensive drug development services

Top-tier CRO with strong presence in European clinical trials market
Strategic position in Amsterdam supporting European clinical operations
Professional environment with emphasis on quality and compliance, supporting work-life balance through hybrid arrangements
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