Senior Statistician (Medical)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
TL;DR
Senior Statistician (SAS/CDISC): Leading biostatistics activities for clinical trials with an accent on statistical analysis plans, sample size calculations, and SAS programming. Focus on designing experimental methods, ensuring CDISC ADaM standards compliance, and validating statistical deliverables to assess drug safety and efficacy.
Location: Saint-Maur-des-Fossés, France
Company
is a global clinical research organization dedicated to bringing new medicines to patients through high-quality medical science services.
What you will do
- Lead all biostatistics activities for clinical trials as the responsible project statistician.
- Develop and review statistical sections of protocols and perform sample size calculations.
- Create statistical analysis plans and document SAS analysis data set structures.
- Develop, program, and validate SAS requirements and statistical deliverables (tables, listings, figures).
- Consult on experimental design and statistical methods for assessing drug product safety and efficacy.
- Collaborate with Data Management and participate in bid defense and kick-off meetings.
Requirements
- MSc in Statistics or equivalent degree.
- Expert knowledge of statistical principles and methods used in clinical research.
- Advanced proficiency in SAS programming and CDISC ADaM standards.
- Strong knowledge of FDA, EMA, and ICH regulations and guidelines.
- English: Proficiency required; CV must be submitted in English.
- Location: Must be based in Saint-Maur-des-Fossés, France.
Culture & Benefits
- Dynamic global environment with over 2,700 dedicated professionals.
- Opportunity to work on the frontline of medical science and impact patient lives.
- Straightforward recruitment process with support at every step.
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