Clinical Study Manager

What You'll Do

• Manage clinical trial timelines, milestones, and deliverables to keep projects on track and on schedule
• Oversee study budgets, forecasting, and financial tracking across multiple vendors and research partners
• Cook up seamless study operations by coordinating with CROs, investigative sites, and internal teams
• Identify and mitigate operational risks before they become roadblocks
• Keep all stakeholders aligned and informed throughout the full trial lifecycle
• Apply your real-world clinical expertise to help evaluate and improve AI-generated clinical research content

Who You Are

• Experienced in clinical trial project management, with a strong command of budgets, timelines, and deliverables
• Skilled at managing vendors, CROs, and external research partners
• Comfortable juggling multiple workstreams and keeping complex, cross-functional studies running without friction
• Detail-oriented and proactive — you anticipate problems and solve them before they escalate
• A clear, confident communicator who can align diverse teams around shared goals

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 data management, or study monitoring