Clinical Statistics Assessment Task Author
Job Description
IXO is engaging specialists to evaluate biostatistical reasoning in clinical research and regulated scientific work. Your contribution is technical work: make the reasoning inspectable, identify substantive errors and provide evidence that supports a reliable assessment.
Work you will do
• Develop or assess cases involving study design, data analysis and the interpretation of clinical or biomedical findings.
• Check methods, assumptions and reporting against the relevant research and regulatory context.
• Provide detailed rubrics, reference explanations and reproducible analytical evidence for the scientific judgment.
Preferred background
• A statistics, biostatistics or epidemiology master's/doctorate and at least four years in pharmaceutical, CRO, hospital or academic-medical work.
• Clinical/observational study design and regulatory documentation, with R, Stata, Python or SAS applied to real clinical data. FDA/EMA-ready submission experience is useful.
• Precise clinical interpretation and detailed technical/rubric writing.
Deliverables
Submit the completed technical artifact or assessment with its supporting evidence, explicit assumptions, reproducible checks where applicable, and concise reasons for each material judgment. Address review findings within the agreed scope.
Location and schedule
Remote assignments are scheduled by agreement, with no guaranteed weekly volume. IXO confirms the applicable timing before work.
Pay and working terms
Per completed task; fee agreed before work USD. Payment is for a completed task that meets the agreed acceptance criteria. The fee, task specification and revision requirements are agreed before work; an advertised time estimate does not determine payment. Applying does not guarantee an assignment. Use public, licensed or otherwise authorized material only; do not submit confidential employer information, personal data or restricted research.