Clinical Study Manager

About the Role

What if your clinical trial management expertise could directly shape how AI understands and navigates the complex world of healthcare research? We're looking for experienced Clinical Study Managers to support the operational execution of clinical studies — and to help train the AI systems that will define the future of medical research.

This is a fully remote, flexible contract role built for seasoned clinical operations professionals who know how to keep complex trials on track. If you've spent time wrangling timelines, managing CROs, and keeping budgets in line across multiple studies, this role was designed for you.

What You'll Do

• Manage clinical trial timelines, milestones, and deliverables to ensure studies stay on track and on budget
• Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and research partners
• Cook up coordination with CROs, clinical sites, and internal teams to ensure smooth, high-quality study execution
• Identify operational risks early, resolve issues efficiently, and keep all stakeholders aligned throughout the trial lifecycle
• Apply your real-world clinical expertise to evaluate and improve AI-generated content related to clinical research workflows
• Work independently and asynchronously — fully on your own schedule

Who You Are

• Experienced clinical trial professional with a strong background in project management, budgets, and timelines
• Proven track record managing CROs, external vendors, or research partners across complex multi-site studies
• Skilled at coordinating multiple workstreams simultaneously without losing sight of quality or deadlines
• Detail-oriented, proactive communicator who keeps stakeholders informed and aligned
• Comfortable working independently in a remote, self-directed environment
• No prior AI or tech background required

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 submissions, GCP compliance, or clinical data management
• Experience across therapeutic areas — oncology, rare disease, or otherwise

Why Join Us

• Work at the intersection of clinical research and cutting-edge AI development alongside leading research labs
• Fully remote and flexible — work when and where it suits you
• Freelance autonomy with the structure of meaningful, impactful project work
• Contribute to AI projects that are shaping the future of healthcare and medical research
• Gain exposure to advanced AI systems and how they're trained using real-world clinical expertise
• Potential for ongoing work and contract extension as new projects launch

Organization

Organization: Alignerr

Type

Type: Hourly Contract

Location

Location: Remote

Commitment

Commitment: 10–40 hours/week