Work as Oncology Clinical Researcher at Alignerr

Expertise in cancer clinical trials could directly shape how AI understands and reasons about oncology — influencing research that affects millions of patients worldwide? We're looking for 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 oncology knowledge embedded in frontier AI systems reflects genuine regulatory, scientific, and clinical standards. This is a fully remote, flexible contract role built for experienced oncology professionals who want to extend their impact beyond the clinic.

Post : Oncology Clinical Researcher

Job Description
• Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment strategies, and regulatory compliance considerations
• Analyze cancer trial data across safety, efficacy, and biomarker endpoints to assess treatment performance and scientific validity
• 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 relevance, and regulatory alignment
• Help establish the standard for how AI models reason about real-world oncology data

Candidate Profile
• Experienced in designing and managing oncology clinical trials — from protocol development through data readout
• Strong analytical background in oncology clinical data, including endpoints, safety profiles, and biomarker interpretation
• Solid familiarity with regulatory submission standards for agencies such as the FDA or EMA
• Detail-oriented and comfortable applying scientific judgment in an independent, asynchronous work environment
• Motivated by the opportunity to influence how AI understands cancer research

Nice to Have
• Prior experience with data annotation, data quality review, or AI evaluation workflows
• Background in translational oncology or biomarker-driven trial design
• Experience preparing or reviewing regulatory submission documents (IND, NDA, BLA, or equivalent)
• Familiarity with AI tools or clinical decision-support systems

Additional Information
Salary : 40-80/hr USD
Location : Remote ; Freelance
Industry Type : Clinical research
End Date : 30th September 2026