Oncology Clinical Researcher
Job in
Dallas, Dallas County, Texas, 75215, USA
Listed on 2026-10-02
Listing for:
Alignerr Corp.
Full Time
position Listed on 2026-10-02
Job specializations:
-
Healthcare
Job Description & How to Apply Below
About
The Role
What if your deep expertise in cancer clinical trials could directly shape how AI reasons about oncology — influencing the tools that will define the next era of cancer research and care? We're looking for experienced Oncology Clinical Researchers to bring real-world clinical rigor into AI-driven research workflows. You'll evaluate, validate, and improve how advanced AI systems understand oncology trial data — ensuring that the science behind cutting-edge AI reflects genuine regulatory, clinical, and scientific standards.
This is a fully remote, flexible contract role built for experienced oncology professionals who want to do meaningful work on their own schedule.
- Organization:
Alignerr - Type:
Hourly Contract - Location:
Remote - Commitment: 10–40 hours/week
- Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment criteria, and regulatory compliance considerations
- Analyze cancer trial data covering safety endpoints, efficacy outcomes, and biomarker results to assess treatment performance
- Translate complex trial outcomes into clear regulatory and scientific narratives aligned with FDA/EMA submission standards
- Review and critique AI-generated oncology insights for clinical accuracy, scientific validity, and regulatory alignment
- Apply your domain expertise to improve how AI models understand and reason about real-world oncology data
- Work independently and asynchronously — fully on your own schedule
- Experienced in designing and managing oncology clinical trials from protocol development through data readout
- Strong background in analyzing clinical oncology data — including primary and secondary endpoints, safety profiles, and biomarkers
- 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 setting
- Comfortable working independently on structured, task-based assignments
- Prior experience with data annotation, data quality evaluation, or AI model assessment workflows
- Background in oncology publications, clinical decision support, or medical writing
- Experience across multiple cancer types or therapeutic modalities
- Work directly on frontier AI systems that are transforming how cancer research is understood and conducted
- Influence how AI models reason about real oncology data — at a scale no individual trial could achieve
- Fully remote and flexible — work when and where it suits you
- Freelance autonomy with the structure of meaningful, impactful work
- Collaborate with world-leading AI research teams and labs
- Potential for ongoing work and contract extension as new projects launch
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