Clinical Trial Biostatistics Evaluation

Reproduce or verify statistical results from clinical datasets and tables. Check estimates, intervals, populations, missing data, censoring and multiplicity against the analysis plan, document the derivation of reference results and distinguish errors from acceptable methodological alternatives.

Professional background

Preferred preparation includes five or more years supporting clinical trials as a biostatistician and an MSc/PhD in statistics, biostatistics or a related quantitative field. Bring direct SDTM/ADaM experience and production or QC of regulatory tables, figures and listings. You should reproduce specified analyses in SAS or R and reconcile reported results with the statistical analysis plan.

Relevant methods

Relevant methods include survival and mixed models, covariate adjustment, multiplicity, missing-data approaches and estimands under ICH E9(R1). Leading pivotal studies, writing CSR statistics sections, oncology endpoints and AI-assisted statistical review are advantages.

Working arrangements

This is remote, paid IXO expert work. Agree the specific task brief, permitted materials, outputs and working schedule with IXO before starting. Any commitment or duration described in a practice profile is an indicative planning requirement for that route, subject to that agreement.

Pay

$65 $70/hr USD. The applicable rate is agreed for the work and professional track before you begin.

Use only materials you are authorized to share, and keep private or restricted information out of your submissions.