Clinical Trial Biostatistics Evaluation

ixolabs.ai; France; Hybride; EUR 78 000 - 84 000; Plein temps

Résumé du poste

ixolabs.ai is seeking an experienced biostatistician to reproduce or verify statistical results from clinical datasets and tables, ensuring they align with the analysis plan. You will check estimates, intervals, populations, missing data, censoring and multiplicity, documenting derivations and distinguishing errors from acceptable alternatives.

Preferred candidates have five or more years supporting clinical trials, an MSc/PhD in statistics or biostatistics, and direct SDTM/ADaM experience with

Qualifications

• Five or more years supporting clinical trials as a biostatistician.
• MSc/PhD in statistics, biostatistics or related quantitative field.
• Direct SDTM/ADaM experience and production or QC of regulatory tables, figures and listings.
• Reproduce specified analyses in SAS or R and reconcile reported results with the statistical analysis plan.

Responsabilités

• 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.
• Lead pivotal studies, CSR statistics sections and oncology endpoints (as described).

Connaissances

Statistical analysis

Clinical trials support

SAS or R proficiency

Regulatory reporting

Data QC

Formation

MSc/PhD in statistics/biostatistics

Outils

SAS

R

ADaM

SDTM

Description du poste

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.

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