Clinical Trial Coordinator

hace 1 mes

Madrid, España Thermo Fisher Scientific A tiempo completo

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. Additional key responsibilities include:Performs investigator file reviews and logging of outstanding issues in project related tracking toolsReviews regulatory documents for proper contentLiaises with monitor and investigative sites to resolve outstanding regulatory issues identifiedDisseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departmentsAssists with the identification of potential investigators and development/distribution of initial protocol packetsCreates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutesQualifications - ExternalEducation and Experience:University degree, or equivalent in education, training and experienceAbility to effectively analyse project specific data/systems to ensure accuracy and efficiencyExperience of manage multiple projects with differing priorities at one given timeExceptional communication, collaboration, organisational and time management skillsFluency in Spanish and English is essentialWhat 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. 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 organisation but with a local feel.How to apply: Please submit your CV in English.#J-18808-Ljbffr

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