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

About the role:

JOB PURPOSE:

Leads and supervises project teams to provide timely programming support in alignment with global project strategies. Assists the supervisor in managing the Chengdu SPAR innovation, Submission Solution team and coordinates cross-departmental collaboration.

 KEY ACCOUNTABILITIES:

•               Leads and supervises project teams to deliver timely and high-quality programming support according to global project strategies.

•               Manages project timelines by developing and maintaining comprehensive project plans, including milestones, task assignments, and coordination of programming activities.

•               Ensures that project teams adhere to departmental standards, processes, and SOPs.

•               Participates in the recruitment and interview process for programmer positions within the department.

JOB-HOLDER ENTRY REQUIREMENTS:

Education:

•               Master's degree in Statistics, Experience & Knowledge:

•               Minimum of 6 years of experience in clinical trial development.

•               Previous experience in project and/or people management is preferred.

•               Strong proficiency in SAS programming and R.

•               Experience supporting at least 20 FDA, EMA, PMDA, or NMPA data submissions.

•               Demonstrated experience (more than 10 projects) in Data Anonymization and Risk Assessment.

Core Competencies:

•               Strong leadership potential to guide cross-functional teams at the study or project level.

•               Excellent English verbal and written communication skills when interacting with internal and external colleagues.

•               Ability to work effectively in a multicultural environment as part of a collaborative team.

•               Solid understanding and application of statistical methods and data analysis techniques.

•               Expertise in preparing data submissions and conducting data anonymization.

•               Proficient in developing and maintaining R packages or R Shiny applications, with flexibility in applying statistical principles.

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!