Clinical Study Coordinator

Stryker; Maastricht; Hybrid; EUR 42,000 - 78,000; Full time

Benefits offered by this job

Incentive compensation

Comprehensive benefits

Job summary

Stryker is seeking a Clinical Study Coordinator to support European clinical trials across Amsterdam, Brussels, and Maastricht with a hybrid work model. You will help manage trial activities, maintain essential documentation, and collaborate with cross-functional teams to ensure quality execution.

Requirements include a Life Sciences degree, 2+ years in clinical research, and GCP experience, plus proficiency in English. Travel is ~10% with potential incentives and comprehensive benefits.

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.

Responsibilities

• 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.

Skills

English proficiency

Education

Bachelor’s degree in Life Sciences or related

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.

Clinical Study Coordinator

• Amsterdam, NH 1012 RJ, Netherlands
• Brussels, Brussels, Belgium
• Maastricht, LI, Netherlands
• Work flexibility: Hybrid
• Employee type: Full Time
• Job category: Clinical Affairs
• Travel: 10%
• Relocation: No

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.
• 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.