Global Clinical Trials 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

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.