Clinical Trial Coordinator Remote
Job description
Clinical Trial Coordinator - United Kingdom (Office based in Cambridge OR Home Based - specific locations)
PPD, part of Thermo Fisher Scientific, are currently hiring for Clinical Trial Coordinators to work in our Cambridge office OR Home based in the following UK locations: Belfast, Bristol, Plymouth/Truro, Norwich/Lincoln. These are strategic locations to support with business needs and CRA development plans.
This role is ideal for a Life Science graduate who wishes to kick start their career within clinical research and grow into a Clinical Research Associate position in the future.
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 programmes. We ensure the highest-quality review of data and effective interaction with study sites, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants.
PPD clinical research service`s mission is to improve health. It starts as an idea to cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our dedicated, forward-thinking and upbeat teams.
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 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 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
University degree in life sciences, or equivalent in education, training and experience
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
Fluency in English
Ability and willingness to be home based in the UK
A valid UK Driving License is advantageous but not essential
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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