Clinical Study Coordinator

Stryker Group; Amsterdam; On-site; EUR 42,000 - 78,000; Full time

Job summary

Stryker Group is seeking a Clinical Research Coordinator to support Europe-wide clinical studies, coordinating essential trial activities and maintaining rigorous study documentation. You will partner with cross-functional teams across the globe to ensure compliant, timely delivery of study milestones.

Ideal candidates hold a life sciences degree with at least 2 years of clinical research experience, proficiency in English, and familiarity with GCP and electronic trial systems.

Qualifications

• Bachelor’s degree in Life Sciences or related field required.
• Minimum 2 years of clinical research or study coordination experience.
• Experience with GCP requirements and regulatory guidelines.
• Experience using electronic clinical trial systems/databases.
• Professional proficiency in English.

Responsibilities

• Coordinate clinical trial activities across the study lifecycle.
• Maintain Trial Master Files and study documentation for inspection readiness.
• Prepare meetings, capture outcomes, and track follow-up actions.
• Review site-related documents and data for accuracy and completeness.
• Manage study invoicing and payment tracking for sites and hospitals.
• Develop and distribute study communications, reports, and newsletters.
• Collaborate with CROs and external partners to support study delivery.
• Ensure compliance with GCP and regulations while managing responsibilities.

Skills

English proficiency

GCP knowledge

Education

Bachelor’s degree in Life Sciences or related

Tools

Trial Master File software

Job description

Join a clinical research team dedicated to generating high-quality clinical evidence that advances patient care. In this role, you will support the successful execution of clinical studies across Europe by coordinating essential clinical trial activities, maintaining study documentation, and partnering with cross-functional teams around the globe. This is an exciting opportunity to contribute to innovative medical device research while working in a highly collaborative international environment.

What You Will Do

• Support clinical trial activities throughout the study lifecycle, including site selection, activation, execution, data collection, and closeout activities.
• Coordinate study documentation and maintain Trial Master Files to ensure inspection readiness and regulatory compliance.
• Prepare study meetings, document meeting outcomes, and track follow-up actions to support study execution.
• Review and process site-related documents, study records, and clinical data for accuracy and completeness.
• Manage study-related invoicing and payment tracking for participating research sites and hospitals.
• Develop, update, and distribute study communications, reports, metrics, and newsletters in partnership with study teams.
• Collaborate with Clinical Program Managers, Clinical Research Associates, Contract Research Organizations, and external partners to support study delivery.
• Ensure compliance with Good Clinical Practice (GCP), applicable regulations, and company procedures while independently managing assigned responsibilities.

What You Will Need

Required Qualifications

• Bachelor’s degree in Life Sciences or a related scientific discipline.
• Minimum 2 years of experience in clinical research, clinical trial administration, study coordination, or a related field.
• Experience working within Good Clinical Practice (GCP) requirements.
• Experience using electronic clinical trial systems, databases, or documentation management systems.
• Professional proficiency in English.

Preferred Qualifications

• Experience supporting medical device clinical trials.
• Experience managing Trial Master Files and essential study documentation. Experience using electronic clinical trial systems, databases, or documentation management systems.
• Knowledge of arterial or venous disease areas, cardiovascular clinical research, or related therapeutic areas.

Netherlands Pay Ranges:

• Netherlands: €42.000 - €78.000 EUR Annual

Belgium Pay Ranges:

• Belgium: €53.500 - €89.100 EUR Annual

At Stryker, we believe transparency helps candidates make confident decisions about their next career step. Compensation is an important part of that process and we want to be clear about how pay is determined. The compensation information posted for this role may be presented as a salary range or a fixed amount depending on the role. In addition to base salary, this role may be eligible for incentive compensation (such as bonus and/or commissions where applicable), along with Stryker’s comprehensive benefits package.

If you’d like to learn more about the salary or the benefits associated with this role, your recruiter will be happy to walk you through the details as you progress through the hiring process.