Clinical Study Manager
ARCHIVED
We can't find an active application page for this role right now. It may reopen or be listed elsewhere. Use Next Steps to search for an active apply link and similar live jobs.
Clinical Study ManagerWhat 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.Organization: AlignerrType: Hourly ContractLocation: RemoteCommitment: 10–40 hours/weekWhat You'll DoManage clinical trial timelines, milestones, and deliverables to ensure studies stay on track and on budgetOversee study budgets, financial forecasting, and cost tracking across multiple vendors and research partnersCoordinate with CROs, clinical sites, and internal teams to ensure smooth, high-quality study executionIdentify operational risks early, resolve issues efficiently, and keep all stakeholders aligned throughout the trial lifecycleApply your real-world clinical expertise to evaluate and improve AI-generated content related to clinical research workflowsWork independently and asynchronously — fully on your own scheduleWho You AreExperienced clinical trial professional with a strong background in project management, budgets, and timelinesProven track record managing CROs, external vendors, or research partners across complex multi-site studiesSkilled at coordinating multiple workstreams simultaneously without losing sight of quality or deadlinesDetail-oriented, proactive communicator who keeps stakeholders informed and alignedComfortable working independently in a remote, self-directed environmentNo prior AI or tech background requiredNice to HavePrior experience with data annotation, data quality review, or evaluation systemsFamiliarity with AI tools or clinical data platformsBackground in regulatory submissions, GCP compliance, or clinical data managementExperience across therapeutic areas — oncology, rare disease, or otherwiseWhy Join UsWork at the intersection of clinical research and cutting-edge AI development alongside leading research labsFully remote and flexible — work when and where it suits youFreelance autonomy with the structure of meaningful, impactful project workContribute to AI projects that are shaping the future of healthcare and medical researchGain exposure to advanced AI systems and how they're trained using real-world clinical expertisePotential for ongoing work and contract extension as new projects launch