Oncology Clinical Researcher

Alignerr Corp.; Tampa (FL); Teletrabalho; USD 83 000 - 165 000; Tempo parcial

Resumo da oferta

Alignerr is seeking an Oncology Clinical Researcher to contribute deep clinical trial expertise to AI training efforts in oncology. The role emphasizes rigorous trial design, data interpretation, and regulatory alignment in a fully remote, hourly-contract setting.

You will collaborate with leading AI teams to ensure oncology data, trial methodologies, and insights meet scientific and regulatory standards while enabling flexible, asynchronous work arrangements.

Qualificações

• Experience designing and managing oncology clinical trials from protocol development through data readout.
• Strong analyst of oncology clinical data, including endpoints, safety, and biomarkers.
• Familiar with FDA/EMA regulatory submission standards.

Responsabilidades

• Design and evaluate oncology clinical trial protocols — including study design, enrollment strategy, and regulatory/ethical compliance.
• Analyze cancer trial data across safety profiles, efficacy endpoints, and biomarker results.
• Translate trial outcomes into regulatory and scientific outputs aligned with FDA, EMA, and other agency submission standards.
• Review and evaluate AI-generated clinical insights for scientific accuracy and regulatory alignment.
• Help shape how frontier AI models understand real-world oncology data.

Conhecimentos

Oncology trials design

Data analysis

Regulatory knowledge

Independent work

Descrição da oferta de emprego

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 systems that may one day transform how cancer is researched and treated worldwide?

We're looking for experienced 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 oncology data, trial methodologies, and clinical insights used to train and evaluate advanced AI systems meet the highest scientific and regulatory standards.

This is a fully remote, flexible contract role built for experienced oncology professionals who want to do meaningful work on their own terms.

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

What You’ll Do

• Design and evaluate oncology clinical trial protocols — including study design, patient enrollment strategy, and regulatory and ethical compliance standards
• Analyze cancer trial data across safety profiles, efficacy endpoints, and biomarker results to assess treatment performance
• Translate clinical trial outcomes into regulatory and scientific outputs aligned with FDA, EMA, and other agency submission standards
• Review and evaluate AI-generated clinical insights for scientific accuracy, clinical relevance, and regulatory alignment
• Help shape how frontier AI models understand, interpret, and reason about real-world oncology data

Who You Are

• Experienced in designing and managing oncology clinical trials from protocol development through data readout
• Strong analyst of oncology clinical data — including primary and secondary endpoints, safety profiles, and biomarker-driven outcomes
• Familiar with regulatory submission standards for agencies such as the FDA or EMA
• Detail-oriented, scientifically rigorous, and comfortable working independently in an asynchronous environment
• Motivated by the idea of applying your clinical expertise to a field that is rapidly redefining cancer research

Nice to Have

• Prior experience with data annotation, data quality evaluation, or AI model assessment workflows
• Background in oncology drug development, translational research, or clinical operations
• Experience producing publications, clinical study reports, or regulatory dossiers

Why Join Us

• Work directly on frontier AI systems being built to transform cancer research and clinical decision-making
• Influence how AI models understand real oncology trial data — your expertise shapes the science
• Fully remote and flexible — work on your own schedule, wherever you are in the world
• Freelance autonomy with access to meaningful, high-impact work at the intersection of oncology and AI
• Collaborate with world-leading AI research labs and teams
• Potential for ongoing work and contract extension as new projects launch