Clinical Study Manager

Overview About The Role What if your clinical trial expertise could directly shape how AI understands and reasons about healthcare research? We are looking for experienced Clinical Study Managers to help oversee and evaluate the operational side of clinical research — bringing real-world expertise to some of the most advanced AI projects in development today. Clinical Study Manager (AI Training) This is a fully remote, flexible contract role designed for seasoned clinical operations professionals who know how to keep complex studies on track. If you\'ve managed trial timelines, wrangled vendor relationships, and kept budgets from spiraling — this role was built for you. Organization: Alignerr Type: Hourly Contract Location: Remote Commitment: 10–40 hours/week What You'll Do Manage clinical trial timelines, milestones, and deliverables to ensure projects stay on track and on schedule Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and research partners Coordinate with CROs, investigative sites, and internal teams to drive smooth, high-quality study execution Identify operational risks early, resolve issues proactively, and keep all stakeholders aligned throughout the trial lifecycle Apply your clinical research expertise to evaluate and improve AI-generated content related to study operations and clinical methodology Who You Are Experienced clinical trial project manager with a strong track record managing budgets, timelines, and deliverables Skilled at coordinating across CROs, external vendors, and internal research teams A natural problem-solver who can untangle complex operational challenges and keep multiple workstreams moving Detail-oriented and methodical — you catch the things others miss 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 content evaluation workflows Background spanning multiple therapeutic areas or trial phases Experience with regulatory documentation, ICH-GCP guidelines, or sponsor oversight Why Join Us Work on cutting-edge AI and healthcare research projects alongside leading AI research labs Fully remote and flexible — work when and where it suits you Freelance autonomy with the structure of meaningful, high-impact project work Gain direct exposure to advanced AI systems and how they\'re trained using real-world clinical research data Potential for ongoing work and contract extension as new projects launch Global collaboration with a diverse, expert community of professionals #J-18808-Ljbffr