Oncology Clinical Researcher

Alignerr; Delhi; A distancia; INR 5.238.000 - 10.476.000; A tiempo parcial

Ventajas ofrecidas por este puesto de trabajo

Fully remote

Flexible schedule

Freelance autonomy

Contract extensions potential

Descripción de la vacante

Alignerr Corp. is seeking an Oncology Clinical Researcher to shape how AI understands and reasons about oncology, ensuring clinical and regulatory standards are embedded in frontier AI systems.

This is a fully remote, hourly contract role for experienced oncology professionals who want to extend impact beyond the clinic, with flexible 10–40 hours per week and opportunities for ongoing collaboration with global AI labs and oncology experts.

Formación

• Experience designing oncology clinical trials from protocol to data readout.
• Strong understanding of regulatory submission standards (FDA/EMA).
• Analytical mindset for safety, efficacy and biomarker data.

Responsabilidades

• Design and evaluate oncology trial frameworks, including study protocols and enrollment strategies.
• Analyze cancer trial data across safety, efficacy and biomarker endpoints.
• Translate trial outcomes into regulatory and scientific narratives for submissions.
• Review AI-generated oncology insights for clinical accuracy and regulatory alignment.
• Help establish how AI models reason about real-world oncology data.

Conocimientos

Oncology trial design

Regulatory submission familiarity

Data interpretation in oncology

Clinical research analysis

Independent remote work

Descripción del empleo

Oncology Clinical Researcher (AI Training)

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?

About The Role

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