Clinical Study Manager

What You'll Do

• Manage clinical trial timelines, milestones, and deliverables to ensure studies stay on track and meet quality standards
• Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and research partners
• Cook with CROs, clinical sites, and internal teams to support smooth execution of trial operations
• Identify operational risks early, resolve issues proactively, and keep all stakeholders aligned throughout the trial lifecycle
• Apply your clinical expertise to evaluate and improve AI-generated content and workflows related to clinical research

Who You Are

• Experienced in clinical trial project management, with a strong command of budgets, timelines, and milestone tracking
• Proven track record managing vendors, CROs, or external research partners
• Skilled at juggling multiple workstreams and keeping complex, multi-site studies running smoothly
• Detail-oriented and systematic — you catch what others miss and document everything clearly
• Self-directed and comfortable working independently in a remote, asynchronous environment

Nice to Have

• Prior experience with data annotation, data quality review, or evaluation systems
• Familiarity with AI tools or clinical data platforms
• Background in regulatory affairs, clinical operations, or healthcare technology
• Experience contributing to process improvement or quality assurance in a research setting