Global Study Coordinator - Netherlands

Who you are

You are driven to achieve goals and looking to make a direct impact in your role. You thrive in a culture where teamwork and communication across departments are valued. Your innovative mindset allows you to bring efficiencies to processes, and you are eager to grow your career in a supportive environment. You understand the importance of managing logistics and patient communications in clinical trials, and you are ready to take on the responsibilities that come with this role.

What you'll do

As a Global Study Coordinator, you will be responsible for supporting the team of Global Study Managers in the planning and operations of active clinical trial studies. You will act as the main point of contact for patient communications, ensuring that all logistical details regarding patient travel are managed effectively. Your role will involve managing the travel and transportation budget for trial participants, participating in discussions with vendors and internal team members, and supporting hospital or clinical staff with trial participant enrollments and visit schedules. You will respond promptly to inquiries from trial participants and clinical staff, contributing to the management of projects to ensure they are delivered efficiently and profitably. Additionally, you will maintain accurate data by setting up databases and transferring information between internal operating systems.

What we offer

This position is part-time, potentially up to 30 hours per week, and pays on an hourly basis. While hours are not guaranteed, you will have the opportunity to work in a dynamic environment where your contributions can make a significant difference. Suvoda values diversity and encourages you to apply even if your experience doesn't match every requirement. You will be part of a team that is committed to improving clinical trial processes and enhancing patient experiences.