Clinical Study Coordinator

Stryker Corporation; Amsterdam, Maastricht; Hybrid; Confidential; Full time

Benefits offered by this job

Hybrid work model

Job summary

Stryker Corporation in Amsterdam, Netherlands is seeking a Clinical Study Coordinator to support European studies. You will coordinate essential trial activities, maintain study documentation, and partner with cross-functional teams worldwide to advance patient care in medical device research.

The role requires a bachelor’s degree in Life Sciences and at least two years’ experience in clinical research, with GCP experience and proficiency in English.

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.
• Professional proficiency in English.

Responsibilities

• Coordinate trial activities across the study lifecycle including site activation, execution, data collection and closeout.
• Maintain Trial Master Files and regulatory documentation for inspection readiness.
• Prepare study meetings, document outcomes and track follow-up actions.
• Review and process site-related documents, study records and clinical data for accuracy.
• Manage study-related invoicing and payment tracking for participating sites and hospitals.
• Develop, update, and distribute study communications and reports with study teams.
• Collaborate with Clinical Program Managers, CRAs, CROs, and external partners to support study delivery.

Skills

Clinical trial coordination

GCP knowledge

English proficiency

Education

Bachelor's degree in Life Sciences

Tools

EDC systems

DMS

Clinical databases

Job description

## Clinical Study CoordinatorApply: Amsterdam, Netherlands: Maastricht, Netherlands: Brussels, Belgium: Full time: Posted Yesterday: R571889Work Flexibility: HybridJoin 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 AnnualAt 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.Travel Percentage: 10%