The Clinical Trial Manager is responsible for the day-to-day regional management of EU study sites and the oversight of CROs for a global Phase 3 program. Key duties include managing site start-up, close-out, and ensuring study conduct aligns with SOPs and regulatory requirements.
Braveheart Bio
3 Remote Job Openings at Braveheart Bio
Lead the planning and execution of EU and ex-U.S. Clinical Trial Applications (CTAs), including managing CROs and CTIS submissions. Coordinate cross-functional deliverables and manage health authority queries to support global development timelines.
The CTMA provides operational and administrative support for a global Phase 3 clinical program, focusing on study coordination and documentation. Key duties include managing site activation, overseeing vendors, and maintaining the Trial Master File (TMF).
