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Clinical Study Coordinator

1 month ago


Leeds, Leeds, United Kingdom Disability Solutions Full time
Clinical Study Administrator Role

At Disability Solutions, we're committed to delivering innovative healthcare solutions. As a Clinical Study Administrator, you'll play a vital role in ensuring the success of our clinical trials.

Key Responsibilities:

Maintain and track relevant activities in our Clinical Trial Management System (CTMS)

Create and distribute regulatory binders, ensuring compliance with applicable regulations and guidelines

Timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies

Support the creation and generation of system reports, providing valuable insights for our study teams

Assist with device tracking and ordering, ensuring seamless supply chain management

About Us:

Disability Solutions is a leading provider of innovative healthcare solutions. Our mission is to empower individuals with disabilities to live independently and with dignity. We're committed to delivering high-quality products and services that make a real difference in people's lives.

Join our team and be part of a dynamic and supportive environment that values innovation, collaboration, and excellence.