Responsibilities
• Create detailed prompts and gold-standard answers across clinical research methodology, interpretation, and scientific communication
• Evaluate and rank AI responses for correctness, rigor, clarity, and contextual relevance
• Review outputs for accuracy, safety, and prompt adherence
• Identify errors in study design, endpoint selection, bias, confounding, statistics, clinical trial methodology, and evidence interpretation
• Fact-check medical and scientific claims and write model solutions that demonstrate correct research reasoning
• Test AI outputs for inaccuracies, misleading evidence interpretation, unsafe recommendations, and bias

Requirements
• Bachelor's degree or higher in Public Health, Epidemiology, Biostatistics, Clinical Research, Biomedical Sciences, PharmD, MD, DO, RN, or a related field
• 5+ years of professional experience in clinical research across academia, hospitals, CROs, biopharma, public health research, or similar settings
• Strong understanding of study design, endpoints, inclusion and exclusion criteria, sample size intuition, and result interpretation
• Comfort evaluating effect sizes, confidence intervals, p-values, multiple comparisons, missing data, and sensitivity analyses
• Deep understanding of bias, confounding, and causality concepts
• Familiarity with clinical trial operations or GCP principles is a plus
• Minimum C1 English proficiency with strong scientific writing skills
• Reliable and self-directed in a remote contractor workflow
• Prior experience in AI data training, medical editorial QA, systematic reviews, or guideline work is strongly preferred

How to Apply
Click "Apply" to be taken to the SME Careers application. Qualified candidates may be added to the expert network for future projects even if no immediate assignment is available.