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Site Monitor II - Job Opportunity at Parexel

Remote, Netherlands
Full-time
Mid-level
Posted: April 10, 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
Career development in clinical research
Global exposure in pharmaceutical industry
Professional training and development

Key Responsibilities

Ensure regulatory compliance and ICH-GCP protocol adherence across clinical trial sites
Conduct comprehensive site monitoring through both remote and on-site methods
Evaluate site performance and develop strategic action plans
Manage source document verification and clinical data accuracy
Oversee protocol deviation reporting and resolution
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 Strong communication and presentation abilities Relationship building capabilities Computer literacy and technology adaptation Protocol compliance assessment
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Sauge AI Market Intelligence

Industry Trends

The clinical research industry is rapidly shifting toward decentralized clinical trials (DCTs) and hybrid monitoring approaches, combining traditional on-site visits with remote monitoring capabilities Increasing adoption of risk-based monitoring (RBM) approaches is transforming the role of Site Monitors, requiring enhanced analytical skills and technology proficiency Growing emphasis on real-world evidence (RWE) and real-world data (RWD) is creating new monitoring challenges and opportunities

Role Significance

Typically works within a team of 5-8 monitors, reporting to a Clinical Research Manager or Project Manager
Mid-level position with significant responsibility for trial quality and compliance, requiring independent judgment and stakeholder management

Key Projects

Phase II-IV clinical trials in multiple therapeutic areas Site initiation and monitoring activities Quality management and compliance initiatives Protocol deviation management and resolution

Success Factors

Strong understanding of clinical research regulations and ICH-GCP guidelines Excellent attention to detail and organizational skills Ability to build and maintain professional relationships with site staff and stakeholders Adaptability to new technologies and monitoring approaches Effective communication across multiple stakeholder levels

Market Demand

High demand with steady growth, driven by increasing clinical trial complexity and regulatory requirements

Important Skills

Critical Skills

ICH-GCP expertise is fundamental for ensuring trial compliance and quality Communication skills are essential for stakeholder management and issue resolution Technical proficiency with clinical trial management systems is crucial for effective monitoring

Beneficial Skills

Project management capabilities enhance career growth potential Therapeutic area expertise can lead to specialization opportunities Risk assessment and analysis skills support modern monitoring approaches

Unique Aspects

Combination of remote and on-site monitoring responsibilities reflects industry evolution
Strong focus on technology adoption and digital transformation in clinical trials
Opportunity to work with global teams and diverse therapeutic areas

Career Growth

2-3 years in current role before advancement, 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) with extensive experience in clinical trial management and biopharmaceutical services

Among the top 5 global CROs with strong presence in Europe and established relationships with major pharmaceutical companies
Strategic position in the Netherlands supporting European clinical trials with growing remote work capabilities
Professional environment with emphasis on quality, compliance, and continuous learning
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