
Lead Biostatistical Programmer
- Boulogne-Billancourt, Hauts-de-Seine
- CDI
- Temps-plein
- Lead statistical programming activities for clinical trials within NITA and I-LCM projects.
- Create and validate ADaM specifications, ADaM datasets, and statistical outputs for CSR, iDMC, ad hoc analyses, and publications.
- Develop and validate CDISC-compliant datasets (ADaM, SDTM) to support regulatory submissions.
- Perform and oversee SAS programming, including development of macros and automated report generation.
- Validate and deliver define.xml, ADRG, and submission packages in accordance with regulatory requirements.
- Ensure compliance with international regulatory and data submission standards.
- Provide strategic oversight and guidance on programming processes and best practices.
- Act as a point of contact for cross-functional stakeholders, ensuring alignment between biostatistics, data management, and clinical teams.
- Mentor and support statistical programmers within the project team.
At Excelya, taking audacious steps is encouraged, so we're looking for individuals who are ready to grow with us and share our values.
- Experience: Advanced technical expertise in statistical programming, with strong proficiency in SAS, proven experience with regulatory and submission guidelines
- Skills: Solid knowledge of CDISC standards (ADaM, SDTM), strong understanding of the drug development lifecycle and functional interfaces, demonstrated ability to lead teams and manage programming activities in a complex, international environment.
- Education: Master's degree in a similar field (Pharma, biostatistics...)
- Languages: Excellent communication skills and fluency in professional English.
Nous sommes désolés mais ce recruteur n'accepte pas les candidatures en provenance de l'étranger.