Impactful European Clinical Trials Coordinator (Hybrid)

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

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.