R&D
Là où votre curiosité fait avancer les miracles de la science

We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

About us

At Sanofi, we chase the miracles of science to improve people’s lives. All our decisions are taken with our most important stakeholder in mind – the patients.

Having a rich history of innovation that dates back over 100 years, Sanofi more than ever stays true to its commitment to transform the practice of medicine by providing potentially life-changing treatments and the protection of life-saving vaccines to millions of people. This history includes the first treatments for many rare diseases and the establishment of standards of care in diabetes and cardiovascular disease. Sanofi’s commitment to public health has helped protect hundreds of millions of people from influenza every year for decades and pushed polio to the brink of eradication, while its scientific vision has led to breakthrough innovations in the treatment of inflammatory diseases.

~ 43.07Bn€ Net Sales FY23

~ 90 countries

~ 91K employees

~ 59 manufacturing sites

~ 20 R&D sites

CoE Associate Manager, Statistical Programming and Analytical Reporting

Leads compound level or multiple studies CoE project and provides high quality and timely delivery of standard datasets, outputs, and e-submission packages.

Major Duties and Responsibilities

ØLead multiple studies and mentor junior programmer.

ØIn cooperation with SP/SB/PPL, plan and timely provide high quality centralized standard programming deliverables utilizing department standard tools and following department SOP’s and guidelines.

ØIn cooperation with CoE PPL, ensure standards implemented consistently across studies at compound level.

ØIn cooperation with the SP/SB, provide the centralized standard programming specifications (including SDTM and ADaM) for a study and implement study metadata.

ØPerform centralized standard programming activities for statistical deliverables.

ØPerform quality control, as required per SOPs, for centralized standard programming deliverables (including input in Validation Plan & QC documentation).

ØProvide standard programming related inputs to e-submission ADaM package and TLG.

ØPrepare items required for e-submission package including SDTM, ADaM and BIMO (FDA only) parts

ØWork closely with study team to provide feedback on study documents from submission perspective, such as dataset metadata file

ØContribute to the submission standard process, template file and tools development/Maintenance.

ØContribute working groups and initiatives e.g. for the development and testing of department tools.

ØReview and provide feedback on study documents as per SOP and RACI requirements.

ØBuild Data standards culture and expertise with readiness to evolving industry standards and regulatory submission requirements.

Required Education/Experience:

·Bachelor's or master's degree in statistics, computer science, or relevant filed

·At least 5 year working experience in clinical trial development

·Ability to support study requirements with challenging timelines under direct supervision by the PPL/PTAH.

·Experience in delivering one or more submisisons to rgulatory authorities globally

·Knowledge on regulatory requirements, understanding of pharmaceutical clinical development and ability to lead regulatory submissions

·Good SAS and R programming skill required

·Experience in Open Source and/or python preferred.

·Great potential/Capability to provide programming leadership to cross -functional teams at the study level

·Effective English verbal and written communication skills in relating to colleagues and associates both inside and outside the organization control approach to work.

·Ability to work effectively in a multi-cultural context as a good team member.

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Toujours Progresser. Découvrir l’Extraordinaire.

Rejoignez Sanofi et entrez dans une nouvelle ère de la science – où votre parcours peut être aussi transformateur que le travail que nous accomplissons. Nous investissons en vous pour que vous alliez plus loin, accélériez votre réflexion et accomplissiez ce qui n’a jamais été fait auparavant. Vous contribuerez à repousser les limites, à bousculer les conventions et à concevoir des solutions plus intelligentes pour les communautés que nous servons. Prêt·e à poursuivre les miracles de la science et à améliorer la vie des gens ? Poursuivons le progrès et découvrons l’extraordinaire – ensemble.

Chez Sanofi, nous croyons dans l’égalité des chances, sans distinction de race, de couleur, d’ascendance, de religion, de sexe, d’origine, d’orientation sexuelle, d’âge, de citoyenneté, d’état civil, de handicap, d’identité de genre ou de tout autre critère protégé par la loi.