Teams at Bright Uro

The Document Control Specialist will manage documentation processes to ensure compliance and organization, collaborating with teams across R&D, Manufacturing, and Regulatory Affairs. Requires attention to detail and excellent communication skills, with an entry-level focus on training for the role.

Support clinical studies across the full lifecycle by monitoring sites, providing real-time case coverage, training site staff on investigational devices, conducting site visits and SDV, maintaining study documentation (TMF, CRFs), tracking enrollment and supplies, and contributing to study documents and publications while ensuring GCP and FDA compliance.