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 design oncology trials and analyze clinical data in alignment with regulatory standards. This remote role offers flexible hours and competitive pay, contributing to transformative AI systems in cancer research. The ideal candidate possesses deep experience in clinical trials, ensuring data integrity and compliance with FDA/EMA protocols. Candidates will enjoy autonomy and potentially extend their contract in a globally collaborative environment.

Benefits

Competitive pay

Flexible remote work

Autonomy and flexibility

Global collaboration

Qualifications

• Deep expertise in cancer clinical trials and data analysis.
• Experience managing trial protocols and patient enrollment.
• Familiarity with regulatory submissions and ethical standards.

Responsibilities

• Design and run oncology clinical trials with oversight on protocols.
• Analyze trial data for treatment efficacy and safety.
• Translate outcomes into regulatory reports for submissions.

Skills

Experience designing oncology clinical trials

Analyzing oncology clinical data

Familiarity with FDA/EMA regulatory standards

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.