Oncology Clinical Researcher

Alignerr Corp.; Delhi; Remote; INR 7,880,000 - 12,476,000; Part time

Job summary

Alignerr is seeking an Oncology Clinical Researcher to shape how AI understands and reasons about oncology knowledge within frontier AI systems. This fully remote, hourly contract role invites experienced oncology professionals to contribute real-world clinical rigor to AI development and regulatory-ready narratives.

You will collaborate with leading AI research teams to ensure oncology content aligns with regulatory and scientific standards, impacting research used worldwide.

Qualifications

• Experience designing and managing oncology clinical trials from protocol development to data readout.
• Strong analytical background in oncology clinical data, endpoints, safety, and biomarkers.

Responsibilities

• 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

Skills

Oncology clinical trial design

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 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.

• Organization: Alignerr
• Type: Hourly Contract
• Location: Remote
• Commitment: 10–40 hours/week

What You'll Do

• 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

Who You Are

• 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

Why Join Us

• Work directly on frontier AI systems that are transforming how cancer research is conducted and understood
• Influence how AI models interpret and reason about real oncology data — a genuinely rare opportunity
• Fully remote and flexible — work on your own schedule, from anywhere
• Freelance autonomy with the structure of meaningful, high-impact project work
• Collaborate with world-leading AI research labs and oncology professionals globally
• Potential for ongoing work and contract extension as new projects launch