Clinical Study Manager
Indexed description
This is a fully remote, flexible contract role designed for seasoned clinical operations professionals who know how to keep complex studies on track, on budget, and running smoothly.
- Organization: Alignerr
- Type: Hourly Contract
- Location: Remote
- Commitment: 10–40 hours/week
- Manage clinical trial timelines, milestones, and deliverables to ensure studies stay on schedule
- Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and partners
- Coordinate with CROs, investigator sites, and internal teams to ensure seamless study operations
- Identify operational risks early, resolve issues decisively, and keep all stakeholders aligned throughout the trial lifecycle
- Apply your real-world clinical expertise to help evaluate and improve AI-generated content related to clinical research
- Experienced in clinical trial project management — you've owned timelines, budgets, and vendor relationships
- Comfortable managing CROs, external research partners, and cross-functional teams simultaneously
- Skilled at juggling multiple workstreams without letting the details slip
- Methodical, proactive, and confident making decisions under pressure
- Clear and effective communicator across technical and non-technical audiences
- Prior experience with data annotation, data quality review, or evaluation systems
- Familiarity with AI tools or research evaluation workflows
- Background in regulatory affairs, clinical data management, or medical affairs
- Work on cutting-edge AI and healthcare research projects alongside world-leading research labs
- Fully remote and flexible — work when and where it suits you
- Freelance autonomy with the structure of meaningful, impactful project work
- Gain exposure to advanced LLMs and how they're trained using real-world clinical data
- Potential for ongoing work and contract extension as new projects launch
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