Oncology Clinical Researcher
- Canada
- Télétravail
- Publié 8 sept. 2026
- 1 poste
- Type d’emploi
- Contrat
- Niveau d’expérience
- Expérimenté · 5+ ans
- Langue de l’offre
- anglais
- Heures de travail
- 40 heures par semaine
- Niveau d’expérience
- Mid-Senior level
Ce poste est expiré
Ce poste chez Alignerr n’accepte plus de candidatures. L’offre originale reste disponible ci-dessous à titre de référence.
Expiré le 17 sept. 2026
Offre d’emploi originale
Evaluate and improve AI-driven research workflows by validating oncology trial data and ensuring scientific and regulatory accuracy. Design clinical trial frameworks and translate complex outcomes into narratives aligned with FDA and EMA standards.
Détails du poste
Oncology Clinical Researcher (AI Training) About The Role What if your deep expertise in cancer clinical trials could directly shape how AI reasons about oncology — influencing the tools that will define the next era of cancer research and care? We're looking for experienced Oncology Clinical Researchers to bring real-world clinical rigor into AI-driven research workflows. You'll evaluate, validate, and improve how advanced AI systems understand oncology trial data — ensuring that the science behind cutting-edge AI reflects genuine regulatory, clinical, and scientific standards. This is a fully remote, flexible contract role built for experienced oncology professionals who want to do meaningful work on their own schedule. Organization: Alignerr Type: Hourly Contract Location: Remote Commitment: 10–40 hours/week What You'll Do Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment criteria, and regulatory compliance considerations Analyze cancer trial data covering safety endpoints, efficacy outcomes, and biomarker results to assess treatment performance Translate complex trial outcomes into clear regulatory and scientific narratives aligned with FDA/EMA submission standards Review and critique AI-generated oncology insights for clinical accuracy, scientific validity, and regulatory alignment Apply your domain expertise to improve how AI models understand and reason about real-world oncology data Work independently and asynchronously — fully on your own schedule Who You Are Experienced in designing and managing oncology clinical trials from protocol development through data readout Strong background in analyzing clinical oncology data — including primary and secondary endpoints, safety profiles, and biomarkers Familiar with regulatory submission standards for agencies such as the FDA or EMA Detail-oriented and rigorous — you hold AI-generated content to the same standards you'd apply in a real clinical setting Comfortable working independently on structured, task-based assignments Nice to Have Prior experience with data annotation, data quality evaluation, or AI model assessment workflows Background in oncology publications, clinical decision support, or medical writing Experience across multiple cancer types or therapeutic modalities Why Join Us Work directly on frontier AI systems that are transforming how cancer research is understood and conducted Influence how AI models reason about real oncology data — at a scale no individual trial could achieve Fully remote and flexible — work when and where it suits you Freelance autonomy with the structure of meaningful, impactful work Collaborate with world-leading AI research teams and labs Potential for ongoing work and contract extension as new projects launch
Ce que vous ferez
Evaluate and improve AI-driven research workflows by validating oncology trial data and ensuring scientific and regulatory accuracy. Design clinical trial frameworks and translate complex outcomes into narratives aligned with FDA and EMA standards.
Exigences
Requires extensive experience in designing and managing oncology clinical trials, including protocol development and data readout. Must be proficient in analyzing safety profiles, biomarkers, and regulatory submission standards.
Compétences indiquées
- Regulatory Compliance · Souhaitée
Autres compétences pertinentes
Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.
- Oncology Clinical Trial Design
- Clinical Data Analysis
- Regulatory Compliance
- FDA Submission Standards
- EMA Submission Standards
- Biomarker Analysis
- Protocol Development
- AI Model Evaluation
- Data Annotation
- Medical Writing
- Clinical Trial Frameworks
- Safety Endpoint Analysis
- Efficacy Outcome Analysis
- Scientific Validation
- Clinical Decision Support
Domaines d’emploi
- Science & Research
- Healthcare
- Technology
- Data & Analytics
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