Clinical Study Manager

What You'll Do

• Manage clinical trial timelines, milestones, and deliverables to ensure studies stay on track from initiation through close-out
• Oversee study budgets, forecasting, and financial tracking across multiple vendors and research partners
• Cook up with CROs, investigative sites, and internal teams to ensure seamless execution of study operations
• Identify operational risks early, resolve issues proactively, and keep all stakeholders aligned throughout the trial lifecycle
• Apply your real-world clinical expertise to evaluate, annotate, and improve AI-generated content related to clinical research workflows

Who You Are

• Experienced in clinical trial project management, with a strong grasp of budgets, timelines, and vendor coordination
• Proven track record managing CROs, external research partners, or multi-site study operations
• Skilled at juggling multiple workstreams while maintaining quality and momentum
• Detail-oriented, methodical, and confident working independently in a remote environment
• Comfortable translating complex operational knowledge into clear, structured outputs

Nice to Have

• Prior experience with data annotation, data quality review, or evaluation systems
• Familiarity with AI tools or clinical data platforms
• Background spanning multiple therapeutic areas or trial phases
• Experience working in decentralized or hybrid trial models