Oncology Clinical Researcher
Alignerr · Columbus, OH
CONTRACT
Posted Sep 7, 2026
Job Description
Oncology Clinical Researcher (AI Training)
About The Role
What if your deep expertise in cancer clinical trials could directly shape how AI understands and reasons about oncology — influencing the tools that could one day transform cancer care for millions of patients?
We're looking for an Oncology Clinical Researcher to bring real-world clinical trial expertise into cutting-edge AI development. You'll evaluate, guide, and validate AI-generated oncology content — ensuring it meets the rigorous scientific, regulatory, and clinical standards that this field demands.
This is a fully remote, flexible contract role built for experienced oncology professionals who want to contribute to something genuinely meaningful — on their own schedule.
- Organization: Alignerr
- Type: Hourly Contract
- Location: Remote
- Commitment: 10–40 hours/week
What You'll Do
- Design and evaluate oncology clinical trial protocols — covering patient enrollment, study design, regulatory compliance, and ethical standards
- Analyze cancer trial data including safety profiles, efficacy endpoints, and biomarker results to assess treatment performance
- Translate trial outcomes into the kind of rigorous scientific and regulatory reporting used for FDA/EMA submissions and clinical decision-making
- Review AI-generated oncology insights and clinical content for scientific accuracy, regulatory alignment, and real-world clinical relevance
- Help shape how frontier AI systems understand, interpret, and communicate complex oncology data
Who You Are
- Experienced in designing and managing oncology clinical trials — from protocol development through to data readout
- Strong working knowledge of oncology clinical data analysis, including endpoints, safety reporting, and biomarker evaluation
- Familiar with regulatory submission standards for agencies such as the FDA or EMA
- Detail-oriented and rigorous — you hold AI-generated content to the same standards you'd apply in a real clinical or regulatory setting
- Comfortable working independently and asynchronously in a remote environment
Nice to Have
- Prior experience with data annotation, data quality evaluation, or AI model assessment workflows
- Background in oncology drug development, medical writing, or clinical operations
- Experience preparing or reviewing regulatory dossiers, clinical study reports, or scientific publications
Why Join Us
- Work directly on frontier AI systems being developed alongside the world's leading AI research labs
- Be among the first oncology experts to influence how AI reasons about real cancer trial data
- Fully remote and flexible — work when and where it suits you
- Freelance autonomy with the substance of genuinely impactful, domain-expert work
- Potential for ongoing work and contract extension as new AI projects launch
About The Role
What if your deep expertise in cancer clinical trials could directly shape how AI understands and reasons about oncology — influencing the tools that could one day transform cancer care for millions of patients?
We're looking for an Oncology Clinical Researcher to bring real-world clinical trial expertise into cutting-edge AI development. You'll evaluate, guide, and validate AI-generated oncology content — ensuring it meets the rigorous scientific, regulatory, and clinical standards that this field demands.
This is a fully remote, flexible contract role built for experienced oncology professionals who want to contribute to something genuinely meaningful — on their own schedule.
- Organization: Alignerr
- Type: Hourly Contract
- Location: Remote
- Commitment: 10–40 hours/week
What You'll Do
- Design and evaluate oncology clinical trial protocols — covering patient enrollment, study design, regulatory compliance, and ethical standards
- Analyze cancer trial data including safety profiles, efficacy endpoints, and biomarker results to assess treatment performance
- Translate trial outcomes into the kind of rigorous scientific and regulatory reporting used for FDA/EMA submissions and clinical decision-making
- Review AI-generated oncology insights and clinical content for scientific accuracy, regulatory alignment, and real-world clinical relevance
- Help shape how frontier AI systems understand, interpret, and communicate complex oncology data
Who You Are
- Experienced in designing and managing oncology clinical trials — from protocol development through to data readout
- Strong working knowledge of oncology clinical data analysis, including endpoints, safety reporting, and biomarker evaluation
- Familiar with regulatory submission standards for agencies such as the FDA or EMA
- Detail-oriented and rigorous — you hold AI-generated content to the same standards you'd apply in a real clinical or regulatory setting
- Comfortable working independently and asynchronously in a remote environment
Nice to Have
- Prior experience with data annotation, data quality evaluation, or AI model assessment workflows
- Background in oncology drug development, medical writing, or clinical operations
- Experience preparing or reviewing regulatory dossiers, clinical study reports, or scientific publications
Why Join Us
- Work directly on frontier AI systems being developed alongside the world's leading AI research labs
- Be among the first oncology experts to influence how AI reasons about real cancer trial data
- Fully remote and flexible — work when and where it suits you
- Freelance autonomy with the substance of genuinely impactful, domain-expert work
- Potential for ongoing work and contract extension as new AI projects launch
Additional Details
- City
- Columbus
- State
- Ohio
- Country
- US
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