At Thermo Fisher Scientific, youll 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 D 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 D 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 tools.
* Reviews regulatory documents for proper content.
* 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 D departments.
* Assists with the identification of potential investigators and development/distribution of initial protocol packets.
* Creates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes.
Qualifications External
Education and Experience:
* University degree, or equivalent in education, training and experience.
* Ability to effectively analyse project specific data/systems to ensure accuracy and efficiency.
* Experience of managing multiple projects with differing priorities at one given time.
* Exceptional communication, collaboration, organisational 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 D clinical research services truly value a work life balance. Weve grown sustainably year on year but continue to offer a collaborative environment, with te