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Site Monitor - FSP - Job Opportunity at Parexel

Amsterdam, Netherlands
Full-time
Mid-level
Posted: March 22, 2025
Hybrid
EUR 45,000 - 65,000 annually based on Amsterdam market rates for clinical research positions

Benefits

Remote work flexibility
Global company exposure
Professional development opportunities
Career advancement in clinical research

Key Responsibilities

Ensure regulatory compliance and ICH-GCP protocol adherence through comprehensive site monitoring
Evaluate and optimize site performance through data-driven assessments
Conduct thorough source document verification and clinical data validation
Manage protocol deviation reporting and remediation
Collaborate with site management teams for operational excellence
Document and report monitoring activities according to established procedures

Requirements

Education

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

Experience

Minimum 1 year experience as clinical monitor

Required Skills

ICH/GCP Guidelines knowledge Clinical trial monitoring expertise CTMS and eTMF system proficiency Local language proficiency English language proficiency Relationship building Communication skills Technology adoption capability Computer proficiency
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Sauge AI Market Intelligence

Industry Trends

Increasing adoption of decentralized clinical trials is driving demand for monitors with remote monitoring capabilities Growing emphasis on real-world evidence and adaptive trial designs requires enhanced analytical skills from site monitors Rising complexity in protocol designs necessitates stronger technical expertise in data management and verification

Role Significance

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

Key Projects

Phase I-IV clinical trials FSP (Functional Service Provider) model implementations Site performance optimization initiatives Protocol compliance programs

Success Factors

Strong attention to detail while maintaining efficient monitoring practices Ability to build and maintain productive relationships with site staff Excellent documentation and reporting capabilities Adaptability to evolving monitoring methodologies

Market Demand

High demand with steady growth due to expanding clinical trial activities in Europe and increasing regulatory requirements

Important Skills

Critical Skills

ICH-GCP knowledge is fundamental for ensuring trial compliance and data integrity Communication skills are essential for effective site management and stakeholder collaboration Technical proficiency in clinical trial management systems directly impacts monitoring efficiency

Beneficial Skills

Project management capabilities enhance career growth potential Experience with multiple therapeutic areas increases versatility Knowledge of risk-based monitoring approaches aligns with industry direction

Unique Aspects

FSP model focus indicates dedicated long-term client relationships
Hybrid monitoring approach shows progressive adaptation to modern clinical trial methods
Strong emphasis on technology adoption and system proficiency

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 CRO providing comprehensive clinical research services across multiple therapeutic areas

Top-tier CRO with strong market presence and established reputation in clinical research industry
Significant European operations with Amsterdam serving as a key hub for clinical research activities
Professional environment with emphasis on quality, compliance, and continuous learning
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