This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.Job DescriptionAt 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 global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start-up to monitoring through to study close-out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies.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.Perform investigator file reviews and logging of outstanding issues in project-related tracking tools.Review regulatory documents for proper content.Liase with monitor and investigative sites to resolve outstanding regulatory issues identified.Disseminate study-related information, including project tracking updates to Clients, clinical study teams, and other PPD departments.Assist with the identification of potential investigators and development/distribution of initial protocol packets.Create meeting agendas and minutes, as well as coordinate team conference calls and distribution of meeting minutes.Qualifications - ExternalUniversity degree, or equivalent in education, training, and experience.Ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency.Experience managing multiple projects with differing priorities at one given time.Exceptional communication, collaboration, organizational, and time management skills.Fluency in Spanish and English is essential.What We Offer:As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance.#J-18808-Ljbffr
