Oncology Clinical Researcher

Alignerr Corp.; Remote; GBP 60,000 - 80,000; Part time

Job summary

A leading AI research firm is seeking an Oncology Clinical Researcher to integrate expertise in cancer trials within AI methodologies. The role involves designing clinical trials, analyzing oncology data for safety and efficacy, and ensuring compliance with regulatory standards. Candidates should have a strong background in oncology research and be familiar with FDA/EMA submission processes. The position offers competitive pay, flexibility, and the opportunity to make a significant impact on AI-driven cancer research.

Benefits

Competitive pay

Flexible remote work

Global collaboration

Qualifications

• Experience in managing all aspects of oncology clinical trials including protocol development.
• Proven ability to analyze cancer trial data including safety, efficacy, and biomarker results.
• Familiarity with regulatory submission standards and previous interaction with FDA or EMA.

Responsibilities

• Design and run trials ensuring compliance with ethical standards.
• Analyze cancer data to evaluate treatment performance.
• Translate outcomes into reports for FDA/EMA submissions.

Skills

Designing oncology clinical trials

Analyzing oncology clinical data

Understanding regulatory standards (FDA/EMA)

Job description

About the Job

At Alignerr, we partner with the world’s leading AI research teams and labs to build and train cutting‑edge AI models. We are seeking an Oncology Clinical Researcher to bring deep expertise in cancer clinical trials into AI‑driven research and evaluation workflows. In this role, you will ensure that oncology trial data used to train and assess advanced AI systems reflects real‑world regulatory, scientific, and clinical standards.

Organization: Alignerr | Position: Oncology Clinical Researcher | Type: Hourly Contract | Compensation: $40–$80 /hour | Location: Remote | Commitment: 10–40 hours/week

What You’ll Do

• Design and run oncology clinical trials by developing study protocols, overseeing patient enrollment, and ensuring compliance with regulatory and ethical standards.
• Analyze cancer trial data, including safety, efficacy, and biomarker results, to evaluate how well treatments perform.
• Translate trial outcomes into regulatory and scientific reports used for FDA/EMA submissions, publications, and clinical decision‑making.
• Review and evaluate AI‑generated clinical insights for accuracy, clinical relevance, and regulatory alignment.

What We’re Looking For

• Experience designing and managing oncology clinical trials from protocol development through data readout.
• Strong background in analyzing oncology clinical data, including endpoints, safety profiles, and biomarkers.
• Familiarity with regulatory submission standards for agencies such as the FDA or EMA.

Preferred

• Prior experience with data annotation, data quality, or evaluation systems.

Why Join Us

• Competitive pay and flexible remote work.
• Work directly on frontier AI systems transforming cancer research.
• Influence how AI models understand and reason about real oncology data.
• Freelance perks: autonomy, flexibility, and global collaboration.
• Potential for contract extension.

Application Process (Takes 15–20 min)

• Submit your resume
• Complete a short screening
• Project matching and onboarding

PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.