Oncology Clinical Researcher

Alignerr Corp.; Chicago (IL); Remote; USD 83,000 - 165,000; Part time

Benefits offered by this job

Fully remote

Freelance autonomy

Contract extension opportunities

Collaborate with AI research teams

Job summary

Alignerr Corp. seeks an Oncology Clinical Researcher to shape AI training for cancer care by supplying regulatory-grounded clinical insights and trial expertise.

You will design and review oncology trial protocols, analyze safety and biomarker data, and translate findings to FDA/EMA submission standards while ensuring AI outputs meet clinical rigor. This remote, hourly contract offers flexible 10-40 hours weekly and the chance to influence frontier medical AI with expert supervision and

Qualifications

• Design and manage oncology clinical trials from protocol to data readout.
• Assess oncology endpoints, safety data and biomarker results.
• Ensure AI outputs align with regulatory standards and clinical rigor.

Responsibilities

• Design and evaluate oncology trial protocols, including enrollment criteria and endpoints.
• Analyze trial data to assess safety, efficacy and biomarker results.
• Translate trial findings into regulatory and scientific outputs aligned with FDA/EMA standards.
• Review AI-generated insights for scientific accuracy and regulatory alignment.
• Provide expert feedback to improve AI model reasoning about oncology data.
• Work independently and asynchronously on flexible schedule.

Skills

Clinical trial design

Oncology expertise

Regulatory knowledge (FDA/EMA)

AI model evaluation

Data annotation & quality

Independent work

Tools

Biostatistics basics

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, reasons about, and advances oncology research? We're looking for Oncology Clinical Researchers to bring real-world clinical knowledge into cutting-edge AI training and evaluation workflows - ensuring the AI systems influencing cancer care are grounded in rigorous, regulatory-grade science.

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

What You'll Do

• Design and evaluate oncology clinical trial protocols, including patient enrollment criteria, endpoint selection, and compliance with regulatory and ethical standards
• Analyze cancer trial data - including safety profiles, efficacy outcomes, and biomarker results - to assess treatment performance and clinical relevance
• Translate trial findings into clear regulatory and scientific outputs aligned with FDA, EMA, or equivalent submission standards
• Review and evaluate AI-generated clinical insights for scientific accuracy, clinical appropriateness, and regulatory alignment
• Provide structured, expert feedback that directly improves how AI models reason about 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 background in analyzing oncology endpoints, safety data, and biomarker results
• Familiar with regulatory submission frameworks for agencies such as the FDA or EMA
• Detail-oriented and methodical - you hold AI-generated content to the same standards you'd apply in a clinical or regulatory setting
• Comfortable working independently on structured, task-based assignments

Nice to Have

• Prior experience with data annotation, data quality evaluation, or AI assessment workflows
• Background in oncology subspecialties such as hematology, immunotherapy, or precision medicine
• Experience authoring or reviewing clinical study reports, IND/NDA submissions, or peer-reviewed publications
• Familiarity with biostatistics or clinical data management

Why Join Us

• Work directly on frontier AI systems transforming how the world understands and fights cancer
• Influence how AI models learn to reason about real oncology data - your expertise shapes the output
• Fully remote and flexible - work when and where it suits you
• Freelance autonomy with the structure of meaningful, expert-level work
• Collaborate with leading AI research teams pushing the boundaries of medical AI
• Potential for ongoing work and contract extension as new projects launch