Clinical Research Jobs at Stryker, Netherlands | Life Sciences Candidates, Apply Online For Clinical Study Coordinator Role
A rare chance to join Stryker, a global leader in medical technologies, as a Clinical Study Coordinator. This role involves supporting clinical studies across Europe, contributing to innovative medical device research while collaborating with international teams. For candidates seeking Clinical Study Coordinator Jobs, this opportunity offers a route to advance in clinical research. Interested candidates should apply before the deadline.
- Job Position: Clinical Study Coordinator
- Location: Amsterdam, NH 1012 RJ, Netherlands; Brussels, Brussels, Belgium; Maastricht, LI, Netherlands
- Job Category: Clinical Affairs
- Req ID: R571889
About The Company
Stryker is a global leader in medical technologies, dedicated to improving healthcare outcomes through innovative products and services in MedSurg, Neurotechnology, and Orthopaedics. The company impacts over 150 million patients annually, working closely with healthcare professionals to enhance patient care and outcomes.
Job Description
Join a clinical research team dedicated to generating high-quality clinical evidence that advances patient care. In this role, the Clinical Study Coordinator 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 position offers an opportunity to contribute to innovative medical device research in a highly collaborative international environment, perfect for those interested in clinical research jobs.
Clinical Study Coordinator 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.
Clinical Study Coordinator Eligibility Criteria
- 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.
Salary
Netherlands Pay Ranges: €42.000 – €78.000 EUR Annual
Belgium Pay Ranges: €53.500 – €89.100 EUR Annual
At Stryker, transparency helps candidates make confident decisions about their next career step. Compensation is an important part of that process, and the company aims 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.
Documents Required
Interested candidates may need to provide relevant academic and professional documents during the application process.
Stryker offers a unique opportunity for qualified candidates to advance their careers in clinical research jobs. With a commitment to improving healthcare outcomes and a collaborative work environment, Stryker encourages interested individuals to apply at the earliest opportunity.
