Oncology Clinical Researcher

Alignerr; Remote; CAD 60,000 - 80,000; Part time

Job summary

A leading AI research partner is seeking an Oncology Clinical Researcher to integrate cancer clinical trials into AI-driven workflows. Responsibilities include designing and overseeing clinical trials, analyzing cancer trial data, and translating outcomes for regulatory submissions. Candidates should have significant experience in oncology trials and familiarity with FDA/EMA standards. This role offers competitive hourly pay and flexible remote work arrangements, along with the opportunity for contract extension.

Benefits

Competitive pay

Flexible remote work

Autonomy and flexibility

Qualifications

• Experience designing and managing oncology clinical trials.
• Strong background in analyzing oncology clinical data.
• Familiarity with FDA or EMA regulatory submission standards.

Responsibilities

• Design and run oncology clinical trials by developing study protocols.
• Analyze cancer trial data to evaluate treatment efficacy.
• Translate trial outcomes into regulatory and scientific reports.
• Review AI-generated clinical insights for accuracy and relevance.

Skills

Designing oncology clinical trials

Analyzing oncology clinical data

Regulatory submission standards

Data annotation

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

Company: 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.