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Site Monitor II - FSP - Job Opportunity at Parexel

Remote, Netherlands
Full-time
Mid-level
Posted: April 8, 2025
Remote
EUR 45,000 - 65,000 annually based on Dutch market rates for clinical research professionals with similar experience

Benefits

Flexible remote work arrangements
Professional development opportunities in clinical research
Global exposure in pharmaceutical industry
Advanced technology and systems access

Key Responsibilities

Ensure regulatory compliance and ICH-GCP protocol adherence through systematic monitoring
Conduct critical site performance evaluations and develop strategic action plans
Execute both remote and on-site monitoring activities per Clinical Monitoring Plan
Manage source document verification and clinical data accuracy
Lead protocol deviation reporting and resolution processes
Collaborate with site management teams for optimal trial execution

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 expertise CTMS and eTMF system proficiency Fluent Dutch and English language skills Networking and relationship building Effective communication Technology adaptation capabilities
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Sauge AI Market Intelligence

Industry Trends

Increasing adoption of decentralized clinical trials is reshaping monitoring roles, requiring expertise in both traditional and virtual oversight methods Growing demand for monitors who can navigate complex regulatory environments across multiple European jurisdictions Rising importance of data integrity and real-time monitoring capabilities in clinical research

Role Significance

Typically works within a team of 5-8 monitors under a clinical operations manager
Mid-level position with significant autonomy in trial monitoring and site management responsibilities

Key Projects

Phase II-IV clinical trials requiring complex protocol management Multi-site international studies requiring cross-border coordination Specialized therapeutic area trials with enhanced monitoring requirements

Success Factors

Strong understanding of European regulatory landscape and ICH-GCP guidelines Ability to balance multiple site relationships while maintaining quality standards Excellence in remote monitoring technologies and virtual collaboration Proactive risk management and issue escalation capabilities

Market Demand

High demand driven by expanding clinical trial activity in Europe and increasing complexity of trial protocols

Important Skills

Critical Skills

ICH-GCP expertise is fundamental for ensuring trial compliance and quality Remote monitoring capabilities are essential in current clinical trial landscape Bilingual proficiency enables effective site communication and documentation

Beneficial Skills

Experience with emerging clinical trial technologies Understanding of risk-based monitoring approaches Knowledge of specific therapeutic areas

Unique Aspects

Combination of remote and on-site monitoring responsibilities reflects evolving industry practices
Strong focus on technology adoption and digital monitoring tools
Emphasis on Dutch language skills indicates important regional market focus

Career Growth

2-3 years in role typically required before advancement to senior positions

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) with extensive experience in managing complex clinical trials

Top-tier CRO with strong presence in European markets and established relationships with major pharmaceutical companies
Strategic position in Netherlands supporting European clinical trial operations
Progressive remote-work environment with emphasis on technological innovation and global collaboration
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