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Alignerr

Oncology Clinical Researcher

Glasgow
$40 – $80/hr
Posted about 9 hours ago
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Oncology Clinical Researcher (AI Training)

About The Role

What if your deep knowledge of cancer clinical trials could directly shape how AI reasons about one of medicine's most complex and high-stakes fields? We're looking for an Oncology Clinical Researcher to bring real-world expertise into the AI development process — ensuring that the models transforming cancer research are grounded in rigorous clinical science.

This is a fully remote, flexible contract role. No prior AI experience needed — just a strong command of oncology trial design, data analysis, and regulatory standards.

Organization: Alignerr
Type: Hourly Contract
Location: Remote
Commitment: 10–40 hours/week

What You'll Do

  • Design and evaluate oncology clinical trial protocols, including patient enrollment criteria, study endpoints, and regulatory compliance frameworks
  • Analyze cancer trial data — covering safety profiles, efficacy results, and biomarker findings — to assess treatment performance and clinical relevance
  • Translate complex trial outcomes into clear, structured outputs aligned with FDA, EMA, and other regulatory submission standards
  • Review and evaluate AI-generated oncology content for scientific accuracy, clinical validity, and regulatory alignment
  • Identify gaps, errors, and inconsistencies in how AI models interpret and represent oncology research

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Who You Are

  • Experienced in designing and managing oncology clinical trials from protocol development through data readout
  • Strong analytical background in oncology data — including endpoints, safety profiles, and biomarkers
  • Familiar with regulatory submission standards for agencies such as the FDA or EMA
  • Detail-oriented and methodical, with a commitment to scientific rigor
  • Able to work independently and deliver consistent, high-quality evaluations

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Nice to Have

  • Prior experience with data annotation, data quality assurance, or AI evaluation workflows
  • Background in translational oncology or clinical pharmacology
  • Experience contributing to peer-reviewed publications or regulatory dossiers

Why Join Us

  • Work directly on frontier AI systems that are transforming how cancer research is understood and applied
  • Influence how AI models reason about real oncology data — your expertise shapes the science
  • Fully remote and flexible — work when and where it suits you
  • Freelance autonomy with the structure of meaningful, task-based work
  • Collaborate with leading AI research labs and teams at the cutting edge of medical AI
  • Potential for ongoing work and contract extension as new projects launch
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Skills

Oncology Trial Design
Data Analysis
Regulatory Standards
Clinical Trial Protocols
Patient Enrollment Criteria
Study Endpoints
Safety Profiles
Efficacy Results
Biomarker Findings
FDA Standards
EMA Standards
Scientific Accuracy
Clinical Validity
Detail-Oriented
Methodical
Independent Work

Location

Glasgow, Scotland, United Kingdom

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