Clinical Study Manager

What You'll Do

• Manage clinical trial timelines, milestones, and deliverables to ensure studies remain on track and on budget
• Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and research partners
• Cook up smooth, high-quality study operations by coordinating with CROs, investigative sites, and internal teams
• Spot operational risks early, resolve issues decisively, and keep all stakeholders aligned throughout the trial lifecycle
• Apply your clinical expertise to evaluate and improve AI-generated content related to clinical research processes

Who You Are

• Experienced clinical trial project manager with a strong command of budgets, timelines, and operational delivery
• Skilled at managing vendors, CROs, and external research partners across complex, multi-workstream studies
• Organised, proactive, and comfortable navigating the fast-moving demands of clinical trial operations
• A clear communicator who can keep diverse stakeholders informed and aligned
• Nice to have: Prior experience with data annotation, data quality review, or evaluation workflows, Familiarity with AI tools or clinical data platforms, Background in regulatory affairs, clinical data management, or medical writing, Experience working across multiple therapeutic areas or global trial settings