Clinical Study Manager
Alignerr · Columbus, OH
CONTRACT
Posted Sep 8, 2026
Job Description
Clinical Study Manager (AI Training)
About The Role
What if your clinical trial expertise could directly shape how AI understands and reasons about healthcare research? We're looking for experienced Clinical Study Managers to bring real-world operational knowledge to cutting-edge AI projects — helping ensure the models influencing the future of medicine are built on accurate, high-quality clinical foundations.
This is a fully remote, flexible contract role. If you have a strong background in clinical trial operations and know what it takes to keep complex studies running on time and on budget, we want to hear from you.
- Organization: Alignerr
- Type: Hourly Contract
- Location: Remote
- Commitment: 10–40 hours/week
What You'll Do
- Oversee clinical trial timelines, milestones, and deliverables to keep studies on track and progressing efficiently
- Manage study budgets, forecasting, and financial tracking across multiple vendors and research partners
- Coordinate with CROs, investigative sites, and internal teams to ensure smooth, high-quality study execution
- 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, or quality-check AI-generated content in the clinical research domain
Who You Are
- Proven background in clinical trial project management — you understand budgets, timelines, and what it takes to deliver
- Experienced in managing CROs, external vendors, or research partners across complex, multi-workstream studies
- Skilled at keeping moving parts organized without letting anything slip through the cracks
- Clear communicator who can align diverse teams around shared goals and timelines
- Self-motivated and comfortable working independently in a remote, asynchronous environment
Nice to Have
- Prior experience with data annotation, data quality assurance, or evaluation workflows
- Familiarity with AI tools or clinical data platforms
- Background in regulatory affairs, clinical operations, or medical research
- Experience working across multiple therapeutic areas or trial phases
Why Join Us
- Work on cutting-edge AI and healthcare research projects alongside leading AI labs and research teams
- Fully remote and flexible — structure your work around your life, not the other way around
- Freelance autonomy with the substance of meaningful, expert-level work
- Gain rare exposure to how advanced AI models are trained using real-world clinical data
- Contribute to work that sits at the intersection of clinical science and the future of AI
- Potential for ongoing work and contract extension as new projects launch
About The Role
What if your clinical trial expertise could directly shape how AI understands and reasons about healthcare research? We're looking for experienced Clinical Study Managers to bring real-world operational knowledge to cutting-edge AI projects — helping ensure the models influencing the future of medicine are built on accurate, high-quality clinical foundations.
This is a fully remote, flexible contract role. If you have a strong background in clinical trial operations and know what it takes to keep complex studies running on time and on budget, we want to hear from you.
- Organization: Alignerr
- Type: Hourly Contract
- Location: Remote
- Commitment: 10–40 hours/week
What You'll Do
- Oversee clinical trial timelines, milestones, and deliverables to keep studies on track and progressing efficiently
- Manage study budgets, forecasting, and financial tracking across multiple vendors and research partners
- Coordinate with CROs, investigative sites, and internal teams to ensure smooth, high-quality study execution
- 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, or quality-check AI-generated content in the clinical research domain
Who You Are
- Proven background in clinical trial project management — you understand budgets, timelines, and what it takes to deliver
- Experienced in managing CROs, external vendors, or research partners across complex, multi-workstream studies
- Skilled at keeping moving parts organized without letting anything slip through the cracks
- Clear communicator who can align diverse teams around shared goals and timelines
- Self-motivated and comfortable working independently in a remote, asynchronous environment
Nice to Have
- Prior experience with data annotation, data quality assurance, or evaluation workflows
- Familiarity with AI tools or clinical data platforms
- Background in regulatory affairs, clinical operations, or medical research
- Experience working across multiple therapeutic areas or trial phases
Why Join Us
- Work on cutting-edge AI and healthcare research projects alongside leading AI labs and research teams
- Fully remote and flexible — structure your work around your life, not the other way around
- Freelance autonomy with the substance of meaningful, expert-level work
- Gain rare exposure to how advanced AI models are trained using real-world clinical data
- Contribute to work that sits at the intersection of clinical science and the future of AI
- Potential for ongoing work and contract extension as new projects launch
Additional Details
- City
- Columbus
- State
- Ohio
- Country
- US
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