An exciting opportunity is available for an experienced Clinical Trials professional to join a high-performing research team supporting the start-up and activation of clinical studies.  This role sits within a dedicated Study Start-Up function and plays a critical part in ensuring trials are launched efficiently, compliantly, and on time. 

The Opportunity
You will take ownership of the end-to-end start-up process, working closely with sponsors, CROs, and internal stakeholders to bring clinical trials from concept to site readiness.

Key Responsibilities

• Act as the primary liaison for Sponsors and CROs during study start-up
• Manage ethics submissions, governance documentation, and CTNs
• Prepare and negotiate budgets and Clinical Trial Research Agreements (CTRA)
• Ensure all regulatory and operational requirements are met prior to site initiation
• Coordinate vendors, systems, and essential document...