Clinical Trial Coordinator

at  Thermo Fisher Scientific

CLINICAL TRIAL COORDINATOR - BRUSSELLS (HYBRID)

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
PPD clinical research services is currently looking for a Clinical Trial Coordinator to join our Clinical Operations in Brussels, Belgium. We will offer you a positive and supportive working environment within one of the most engaged teams in the industry. We will provide you with meaningful and challenging work and the opportunity to acquire valuable personal and professional skills, through our best-in-class training and development.
As a Clinical Trial Coordinator, you will provide support to the project team. Will coordinate non-clinical responsibilities of project administration as applicable to the client contract under the direction of the assigned Clinical Manager or Sr. Clinical Manager.

• Reviews regulatory documents for proper content
• Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools
• Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified
• Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments
• Assists with the identification of potential investigators and development/distribution of initial protocol packets
• Creates meeting agendas and minutes
• Coordinates team conference calls and distribution of meeting minutes