At Sanofi, we have a shared commitment to bring innovation and rigor to clinical development.

As a biomarker Statistical Programmer, you will play a key role in supporting a growing pipeline focused on oncology, immunology & inflammation, rare disease, and rare blood disease, with emphasis on trial conduct, innovative-driven solutions, and regulatory submissions.

You will provide leadership and guidance at the study and project level, accountable for the plan and execution of biomarker programming activities, including support of fast ongoing decision making (early phase).

You do not feel comfortable yet with all these expectations and really want to grow to embrace these responsibilities? Let’s get in touch, you will be supported by a Biostatistics and Programming Department that fosters people development, offering compelling career opportunities that value diversity of thought and abilities, to optimize overall success and have a meaningful impact on patients’ lives

Major Duties and Responsibilities:

Biomarker programming study lead of several studies: plan and execute statistical programming activities for the accountable study.

• Perform programming activities, including ADaMs, Tables/Listings/Figures (TLFs) and support documentation for all statistical deliverables (e.g., interim analyses, publications, exploratory analyses) within a study/project
• Perform quality control for statistical programming deliverables
• Review and provide feedbacks on study documents, such as Case Report Form (CRF), Statistical Analysis Plan (SAP) and Table Listing and Figures (TLF) templates.
• Propose innovative solutions to faster provide statistical deliverables

Required Education/Experience:

• Post-graduate with at least 3+ (study lead) of programming experience in processing clinical trial data in the pharmaceutical industry
• Technical skills in statistical programming (e.g., SAS, R)
• Familiar with biomarker related CDISC standard
• Experience with high dimensional data (and machine learning algorithms, if possible)
• Experience with biomarker data, in particular complex biomarker data such as omics
• Knowledge on regulatory requirements understanding of pharmaceutical clinical development and ability to lead regulatory submissions
• Good communications and negotiation skills
• Ability to have efficient exchanges with partners, service providers, and colleagues across geographical locations
• Represent Sanofi in external communication: congresses, international working groups
• Strong skills that demonstrate initiative, motivation, and teamwork in global interdisciplinary teams
• Ability and mindset to embrace change, innovate and continuously improve programming practice

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.