About this opportunity
Alignerr Corp. lists this Clinical Study Manager opportunity in sheffield, Texas. Review the employer’s description below for duties, qualifications and application requirements.
Job description
About The Role
What if your expertise in clinical trial operations could directly shape how AI understands and supports the future of healthcare research? We're looking for experienced Clinical Study Managers to help oversee the operational execution of clinical trials — ensuring studies are delivered on time, within budget, and to the highest quality standards — while contributing to some of the most advanced AI research being done today.
Clinical Study Manager (AI Training)
About The Role
What if your expertise in clinical trial operations could directly shape how AI understands and supports the future of healthcare research? We're looking for experienced Clinical Study Managers to help oversee the operational execution of clinical trials — ensuring studies are delivered on time, within budget, and to the highest quality standards — while contributing to some of the most advanced AI research being done today.
This is a fully remote, flexible contract role built for seasoned clinical operations professionals who want meaningful work on their own terms.
Organization: Alignerr
Type: Hourly Contract
Location: Remote
Commitment: 10–40 hours/week
What You'll Do
Manage clinical trial timelines, milestones, and deliverables to keep studies on track and on schedule
Oversee 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 help train and evaluate AI models built for healthcare and life sciences applications
Who You Are
Experienced in clinical trial project management — you know how to keep complex studies moving across budgets, timelines, and teams
Skilled at managing vendors, CROs, and external research partners with confidence
Able to coordinate multiple workstreams simultaneously without losing sight of quality or detail
Clear, structured communicator who can keep stakeholders informed and aligned
Self-directed and reliable when working independently in a remote environment
Nice to Have
Prior experience with data annotation, data quality review, or evaluation systems
Background working across multiple therapeutic areas or trial phases
Familiarity with AI tools or clinical data platforms
Why Join Us
Work at the intersection of clinical research and cutting-edge AI — a genuinely rare opportunity
Fully remote and flexible — structure your hours around your life
Freelance autonomy with the substance of high-impact, meaningful work
Collaborate with world-leading AI research teams and labs
Gain firsthand exposure to how advanced AI models are trained using real-world clinical data
Potential for ongoing work and contract extension as new projects launch
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.