Global Clinical Trial Manager — Operations & Compliance

ICON Clinical Research; Netherlands; Remote; EUR 70,000 - 100,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

LifeWorks, global EAP, 24/7 support

Life assurance

Childcare vouchers / bike purchase / 0

Job summary

ICON Strategic Solutions in the Netherlands is seeking a Clinical Trial Manager to lead day-to-day clinical trial management across our sponsor-dedicated model. You will support teams to deliver high-quality outcomes for multiple clinical programmes, coordinating with investigators and stakeholders to ensure timelines, budgets, and regulatory compliance.

You will build strong cross-functional relationships, drive trial deliverables, and lead a geographically diverse team.

Qualifications

• University degree in medicine, science, or equivalent combination of education & experience.
• Demonstrated ability to drive the clinical deliverables of a study.
• Subject matter expertise in the designated therapeutic area.
• Prior monitoring experience is preferred.
• Willingness to travel as required (approximately 25%)

Responsibilities

• Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
• Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
• Build and manage strong relationships with trial investigators and stakeholders.
• Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
• Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Skills

Clinical trial management

Stakeholder management

Regulatory compliance

Team leadership

Travel readiness

Education

University degree in medicine or science

Tools

GCP/ICH knowledge

Job description

ICON Strategic Solutions in the Netherlands is seeking a Clinical Trial Manager to lead day-to-day clinical trial management across our sponsor-dedicated model. You will support teams to deliver high-quality outcomes for multiple clinical programmes, coordinating with investigators and stakeholders to ensure timelines, budgets, and regulatory compliance.

You will build strong cross-functional relationships, drive trial deliverables, and lead a geographically diverse team.