Clinical Statistics Assessment Task Author

ixolabs.ai; France; Hybride; Plein temps

Résumé du poste

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.

Location is remote; deliverables include detailed rubrics, reference explanations and reproducible analytical evidence for the scientific judgment across study designs and regulatory contexts.

Qualifications

• Masters/doctorate in statistics/biostatistics/epidemiology or equivalent.
• At least four years in pharmaceutical, CRO, hospital or academic-medical work.
• Experience with regulatory submissions (FDA/EMA) is useful.

Responsabilités

• Develop or assess cases involving study design, data analysis and interpretation of findings.
• Check methods, assumptions and reporting against the regulatory context.
• Provide rubrics, explanations and reproducible evidence for scientific judgment.

Connaissances

Biostatistics expertise

Clinical interpretation

Formation

Statistics/biostatistics/epidemiology master's/doctorate

Outils

R

Stata

Python

SAS

Description du poste

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.