- Experience
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- Salary
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- Openings
- 1
- Posted
- 2 days ago
Job description
About the Role
This contract position is designed for seasoned oncology clinical research specialists who want to apply their trial and regulatory expertise to AI development. The work involves helping ensure that AI systems handling cancer-related information are accurate, scientifically grounded, and aligned with clinical standards.
The arrangement is fully remote, flexible, and suited to professionals who prefer project-based collaboration while continuing to work within their specialty.
Role Details
- Organization: Alignerr
- Engagement type: Hourly contract
- Work arrangement: Remote
- Expected commitment: 10 to 40 hours per week
What You Will Do
- Check AI-produced oncology material for medical accuracy, scientific reliability, and consistency with regulatory expectations.
- Use your knowledge of oncology trial planning, including protocol creation, patient recruitment, and endpoint definition, to judge whether AI reflects real-world research practice.
- Assess trial-related outputs such as safety data, efficacy findings, and biomarker results, and identify reasoning mistakes or missing details.
- Compare AI-generated scientific and regulatory write-ups with FDA, EMA, and ICH requirements.
- Deliver organized expert feedback that helps improve how AI models interpret oncology evidence and clinical decision-making.
- Work independently on an asynchronous schedule.
Who This Role Suits
We are seeking professionals who have hands-on experience in planning and managing oncology clinical trials from protocol development through final data interpretation. The ideal candidate can confidently analyze oncology evidence, is familiar with regulatory submission standards, and works carefully when reviewing complex scientific content. Comfort with remote, task-based work is also important.
Preferred Background
- Experience in data annotation, data quality checks, or AI evaluation.
- Exposure to translational oncology or regulatory/clinical writing.
- Knowledge of biomarker-led study design or precision oncology.
- Familiarity with AI tools or content review platforms.
Why Join
- Contribute to advanced AI systems that are reshaping cancer research.
- Help improve how future models interpret oncology data, clinical standards, and regulatory science.
- Enjoy a fully remote and flexible work setup.
- Benefit from the independence of freelance-style work while doing meaningful expert-level tasks.
- Work alongside leading AI research teams and labs.
- There is potential for continued assignments and contract renewal as additional projects begin.
Additional Information
This opportunity is an hourly contract role based in remote work. The expected weekly workload ranges from 10 to 40 hours. The position is intended for experienced oncology professionals contributing to AI training and evaluation work.