Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Clinical Trial Coordinator - Ede, Netherlands (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.
Our clinical department defines, develops and delivers clinical programs, ensuring the highest-quality review of data and effective interaction with study sites.
As a Clinical Trial Coordinator, you will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable to the client contract. Additional key responsibilities include:
* Performs PPD investigator file reviews and logs outstanding issues in project tracking tools.
* Reviews regulatory documents for proper content.
* Liaises with monitors and investigative sites to resolve outstanding regulatory issues.
* 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 the development/distribution of initial protocol packets.
* Prepares meeting agendas and minutes, coordinates team conference calls, and distributes meeting minutes.
Education and Experience:
* University degree or equivalent in education, training, and experience.
* Responsible for adhering to Good Clinical Practices, country-specific regulations, PPD/Client Standard Operating Procedures, and Working Practice Documents for all non-clinical/clinical aspects of project implementation, execution, and closeout.
* Ability to effectively analyze project-specific data and systems to ensure accuracy and efficiency.
* Experience managing multiple projects with differing priorities simultaneously.
* Outstanding communication, teamwork, organizational, and time management skills.
* Proficiency in English and Dutch languages.
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