Oncology Clinical Researcher

Alignerr Corp.; Remote; GBP 80,000 - 100,000; Part time

Job summary

A leading AI research company based in the UK is seeking an Oncology Clinical Researcher to oversee oncology clinical trials and analyze data to support AI-driven evaluation workflows. This role is remote and offers competitive pay ranging from $40 to $80 per hour, requiring expertise in cancer trials and regulatory standards. The ideal candidate will have a strong background in managing clinical trials and translating outcomes for regulatory submissions. Join a team influencing AI understanding of oncology data.

Benefits

Competitive pay

Flexible remote work

Freelance autonomy

Qualifications

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

Responsibilities

• Design and run oncology clinical trials ensuring compliance with regulatory standards.
• Analyze cancer trial data to evaluate treatment performance.
• Translate trial outcomes into regulatory reports for submissions.

Skills

Designing oncology clinical trials

Analyzing clinical data

Familiarity with regulatory submissions

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.