Oncology Clinical Researcher at Alignerr — NeverHard
Oncology Clinical Researcher at Alignerr in Toronto, Ontario. Skills: AI, Clinical Trials, Oncology, Regulatory Compliance, Scientific Research. Apply on NeverHard.
Company
Alignerr
Location
Toronto, Ontario
Type
contract
Remote: Yes
Required skills:
AI
Clinical Trials
Oncology
Regulatory Compliance
Scientific Research
Oncology Clinical Researcher (AI Training)About The Role
What if your expertise in cancer clinical trials could directly shape how AI understands and reasons about oncology — influencing the tools that may one day transform how cancer is diagnosed and treated?
We're looking for Oncology Clinical Researchers to bring deep, real-world clinical trial knowledge into cutting-edge AI development. You'll work alongside leading AI research teams to ensure that the oncology data, insights, and reasoning powering next-generation AI systems are scientifically rigorous, clinically accurate, and regulatory-compliant.
This is a fully remote, flexible contract role. No AI background required — just deep expertise in oncology clinical research and a sharp eye for scientific 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 — protocols, patient enrollment, endpoints, and compliance — to assess and improve AI outputs
Analyze how AI handles cancer trial data, including safety profiles, efficacy results, and biomarker findings
Evaluate AI-generated regulatory and scientific content against FDA/EMA submission standards
Provide structured, expert feedback that directly shapes how AI models reason about real-world oncology
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 background in analyzing oncology clinical data, including endpoints, safety profiles, and biomarkers
Familiar with regulatory submission standards for agencies such as the FDA or EMA
Detail-oriented and methodical, with high standards for scientific accuracy
Able to clearly articulate complex clinical reasoning in written evaluations
No prior AI or tech experience required
Nice to Have
Prior experience with data annotation, data quality review, or AI evaluation workflows
Background in translational oncology, biomarker research, or regulatory affairs
Experience contributing to peer-reviewed publications or clinical decision-making frameworks
Why Join Us
Work directly on frontier AI systems with the potential to transform cancer research and care
Influence how AI models understand, interpret, and reason about real oncology data
Fully remote and flexible — work when and where it suits you
Freelance autonomy with the structure of meaningful, high-impact work
Collaborate with world-leading AI research teams and labs
Potential for ongoing work and contract extension as new projects launch