Description
We are seeking a Study Coordinator to facilitate study setup, including protocol and budget review, leading meetings, and developing project plans. You will partner with the Study Setup team for quality database setup and oversee protocol documentation. Your responsibilities will include preparing and presenting protocol-specific materials at Kick Off and Investigator meetings, monitoring project plans, timelines, and deliverables, managing documentation, and overseeing study monitoring and reporting.
You will manage study scope changes and budget, monitor quality of the study and any service-related issues, implementing changes as required. Collaboration with project management to improve processes and service quality is also essential. You will coordinate company services such as database setup, data management, and lab operations, serving as a resource for internal departments.
The ideal candidate will have a Bachelor's degree in Life Sciences or a related field, knowledge of project management methodologies, and a minimum of 18 months of experience in a project management and customer-facing environment. Experience in the clinical or research industry is highly desirable.
In return, you will have access to global exposure, variety of therapeutic areas, a collaborative and supportive team environment, cutting-edge technology, excellent career development opportunities, and a strong focus on work-life balance and well-being.