This is an exciting opportunity with candidates to start and interview as soon as possible!
The Clinical Study Coordinator must have minimum 1/2 years' clinical research experience as they need an individual who can work independently as well as part of a team. Day to day responsibilities will involve a reporting adverse events, data entry, administrative tasks and query resolution.
Nice to have:
Multiple Myeloma experience
Clinical Research Coordinator in Reading employer: Actalent
Actalent is an excellent employer, offering a dynamic work environment in Dunton where innovation meets automotive excellence. Employees benefit from a culture that prioritises collaboration and professional growth, with access to advanced engineering projects that shape the future of powertrains. Join us to be part of a team that values your expertise and fosters continuous learning in a state-of-the-art facility.
