Clinical Trial Coordinator – Copenhagen, Denmark 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. Location/Division Specific Information Do you want to be part of the vital links between an idea for new medicine and help the people who need it? Are you motivated by the opportunity to grow within a global organization? At PPD Clinical Research Group we are thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to enable our customers to make the world healthier, cleaner, and safer. You will be joining a truly collaborative and winning culture as we strive to bend the time curve of delivering life-saving therapies to patients. Our Danish office consists of colleagues with in-depth therapeutic experience, people with various educations within life science and both newly educated people plus people with years of experience. All in all, we have a very dynamic environment where initiative, flexibility, responsibility, commitment, and fun are in focus. A day in the Life: Performs PPD clinical research services investigator file reviews and logging of outstanding issues in project related tracking tools – Reviews regulatory documents for proper content – Liaises with monitorand investigative sites to resolve outstanding regulatory issues identified – Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD clinical research services departments – Assists with the identification of potential investigators and development/distribution of initial protocol packets – May assist the project team with the preparation of regulatory compliance review packages – Builds meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes Education – University degree, or equivalent in education, training and experience Knowledge, Skills, Abilities Responsible for adhering to Good Clinical Practices, country specific regulations, PPD clinical research services /Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout – Ability to effectively analyse project specific data/systems to ensure accuracy and efficiency – Experience of manage multiple projects with differing priorities at one given time – Outstanding communication, teamwork, interpersonal and time management skills – Excellent command of the English language and the language where the position is located What we offer: At PPD Clinical Research Group we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore you will benefit from our award-winning learning and development program, ensuring you reach your potential. We have an adaptable working culture, where we truly value a good work-life balance. We’ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel. If you resonate with our 4i values – Integrity – Innovation – Intensity – Involvement – and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, submit your application today.