Oncology Clinical Researcher

Alignerr; Raleigh (NC); A distancia; USD 83.000 - 165.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Fully remote

Freelance autonomy

Flexible schedule

Descripción de la vacante

Alignerr Corp. is seeking an Oncology Clinical Researcher to shape how AI understands oncology content through rigorous review and regulatory alignment.

This fully remote, hourly contract role offers flexible 10–40 hours per week, letting you apply deep clinical expertise on your schedule. You will evaluate AI-generated oncology material, refine study designs, and provide expert feedback to improve model reasoning.

Formación

• Experience designing and managing oncology clinical trials from protocol through data readout.
• Strong analytical background in oncology clinical data, endpoints, safety, and biomarkers.
• Familiarity with regulatory submission standards for FDA, EMA, or comparable agencies.
• Detail-oriented, systematic thinker who communicates clinical reasoning clearly.

Responsabilidades

• Review AI-generated oncology content for clinical accuracy and regulatory alignment.
• Assess trial design elements: protocols, endpoints, enrollment logic, compliance.
• Analyze AI outputs on safety signals, efficacy, and biomarker findings.
• Evaluate AI insights against real-world regulatory standards.
• Provide structured expert feedback to improve AI model understanding.
• Work independently and asynchronously on task-based assignments.

Conocimientos

Oncology clinical trials

Trial design

Regulatory standards (FDA/EMA)

Clinical data review

Regulatory alignment

Descripción del empleo

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 could one day save lives at scale?

We're looking for Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI development. You'll review, evaluate, and help refine AI-generated oncology content — ensuring it reflects the scientific, regulatory, and clinical standards that matter most in cancer research.

This is a fully remote, flexible contract role built for experienced oncology professionals who want to contribute to something genuinely transformative — on their own schedule.

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

What You'll Do

• Review and evaluate AI-generated oncology content for clinical accuracy, scientific validity, and regulatory alignment
• Apply your trial design expertise to assess study protocols, endpoint definitions, patient enrollment logic, and compliance frameworks
• Analyze AI outputs covering cancer trial data — including safety signals, efficacy results, and biomarker findings — and flag gaps or errors
• Evaluate how well AI-generated insights reflect real-world regulatory standards for agencies such as the FDA and EMA
• Provide structured, expert feedback that directly improves how AI models understand and reason about oncology data
• Work independently and asynchronously on task-based assignments — fully on your own schedule

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 biomarkers
• Familiar with regulatory submission standards for the FDA, EMA, or comparable agencies
• Detail-oriented and systematic — you notice when clinical or scientific logic doesn't hold up
• Clear and precise written communicator who can articulate complex clinical reasoning
• Comfortable working independently without day-to-day oversight

Nice to Have

• Prior experience with data annotation, data quality evaluation, or AI content review
• Background in translational oncology, biomarker research, or precision medicine
• Experience contributing to regulatory submissions, clinical study reports, or scientific publications
• Familiarity with AI tools or clinical informatics platforms

Why Join Us

• Work directly on frontier AI systems being built to transform cancer research and clinical decision-making
• Influence how AI models interpret real oncology data — your expertise shapes what these systems get right
• Fully remote and flexible — work when and where it suits you, with no fixed schedule
• Freelance autonomy with the structure of meaningful, expert-level work
• Collaborate with world-leading AI research teams and labs on problems that matter
• Potential for ongoing work and contract extension as new projects launch