About this opportunity
Alignerr lists this Oncology Clinical Researcher opportunity in indianapolis, Indiana. Review the employer’s description below for duties, qualifications and application requirements.
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 research that could one day impact millions of patients?
We're looking for experienced Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI development. You'll work alongside leading AI research teams to ensure that the systems being built to transform cancer research are grounded in accurate, regulatory-aligned, and scientifically sound clinical knowledge.
This is a fully remote, flexible contract role. No AI background needed - just deep oncology expertise and a sharp eye for clinical quality.
Organization
: Alignerr
Type
: Hourly Contract
Location
: Remote
Commitment
: 10-40 hours/week
What You'll Do Review and evaluate AI-generated oncology content for clinical accuracy, scientific validity, and regulatory alignment
Apply your expertise in trial design - including protocol development, patient enrollment standards, and ethical compliance - to assess and improve AI outputs
Analyze AI-generated interpretations of cancer trial data, including safety profiles, efficacy endpoints, and biomarker findings
Evaluate how well AI systems translate trial outcomes into regulatory and scientific contexts relevant to FDA/EMA standards
Provide structured, expert feedback that directly shapes how frontier AI models reason about real oncology data
Work independently and asynchronously - fully on your own schedule
Who You Are Experienced in designing and managing oncology clinical trials from protocol development through data readout
Strong command of oncology clinical data analysis - endpoints, safety profiles, biomarkers, and beyond
Solid familiarity with regulatory submission standards for agencies such as the FDA or EMA
Naturally detail-oriented with a rigorous, systematic approach to evaluating clinical information
Able to communicate complex clinical findings clearly and concisely in written form
No prior AI or tech experience required
Nice to Have Prior experience with data annotation, data quality assessment, or AI evaluation workflows
Background in translational oncology, clinical pharmacology, or regulatory affairs
Experience authoring or reviewing clinical study reports, IND/NDA submissions, or publications
Familiarity with AI tools or clinical decision support platforms as an end user
Why Join Us Work directly on frontier AI systems that are transforming how cancer research is conducted
Fully remote and flexible - work when and where it suits you
Freelance autonomy with the structure of meaningful, high-impact project work
Influence how AI models understand, evaluate, and reason about real-world oncology data
Collaborate with world-leading AI research teams and labs
Potential for ongoing work and contract extension as new projects launch
Worksite address
indianapolis, IN, 46262, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.