About the Role
What if your clinical trial management expertise could directly shape how AI understands and reasons about one of the most complex, high-stakes fields in the world? We're looking for experienced Clinical Study Managers to help build and validate AI systems trained on real-world clinical research data — bringing rigor, precision, and operational know-how to the frontier of AI development.
This is a fully remote, flexible contract role. You'll apply your deep knowledge of clinical trial operations to evaluate, annotate, and improve AI outputs — helping ensure these models reflect the standards and realities of professional clinical research.
- Organization: Alignerr
- Type: Hourly Contract
- Location: Remote
- Commitment: 10–40 hours/week
What You'll Do
- Oversee and evaluate AI-generated content related to clinical trial operations, timelines, budgets, and vendor management
- Apply your real-world clinical research expertise to assess the accuracy, completeness, and quality of AI outputs
- Manage and review simulated or real clinical trial workflows, milestones, and deliverables as part of AI training datasets
- Identify gaps, errors, and inconsistencies in AI-generated clinical research content and provide structured, detailed feedback
- Coordinate across multiple workstreams to ensure study-related AI tasks are completed on time and to a high standard
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Experienced clinical trial professional with a strong background in study operations and project management
- Skilled at managing budgets, timelines, and vendor or CRO relationships across complex, multi-site studies
- Naturally detail-oriented with a systematic approach to identifying risks and resolving operational issues
- Clear and confident written communicator who can document findings precisely
- Self-motivated and reliable when working independently without close supervision
Nice to Have
- Prior experience with data annotation, data quality review, or AI evaluation workflows
- Familiarity with eClinical systems, EDC platforms, or clinical data management tools
- Background in regulatory affairs, GCP compliance, or clinical operations leadership
- Experience working across therapeutic areas or international multi-site trials
Why Join Us
- Work on cutting-edge AI projects alongside leading AI research labs and healthcare innovators
- Fully remote and flexible — work when and where it suits you
- Freelance autonomy with the structure of meaningful, high-impact work
- Gain exposure to advanced large language models (LLMs) and how they're trained using real-world clinical expertise
- Contribute to AI development that has a genuine impact on the future of healthcare and clinical research
- Potential for ongoing work and contract extension as new projects launch