R&D - CSO - Associate Manager, Statistical Programming and Analytical Reporting - CD
Synthorx
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
JOB PURPOSE:
Leads and supervises project teams to provide timely programming support according to global project strategies.
Assist supervisor in managing the Chengdu Statistical Programming innovation team and completed the cross-department coordinate work
SUPERVISED RESOURCES:
KEY ACCOUNTABILITIES:
Ø Leads and supervises project teams to provide timely programming support according to global project strategies.
Ø Project management, provides and maintain project plan for projects/study including milestones, tasks, and coordination of programming activities
Ø Ensures project teams adherence to department standards, processes and SOPs
Ø Contributes to the recruitment and interview process for programmer positions within the department.
JOB-HOLDER ENTRY REQUIREMENTS:
Education:
Master degree in statistics, computer science
Experience & knowledge:
Ø At least 5 year working experience in clinical trial development
Ø Previous project/people management experience preferred
Ø Good SAS programming and R skill required
Ø Experience with at least 5 FDA, EMA, PMDA or NMPA data submissions or support
Ø Data Anonymization and Risk Assessment and more then 60 projects implement experience
Core competencies:
Ø Great potential/Capability to provide programming leadership to cross -functional teams at the study and or project level
Ø Effective English verbal and written communication skills in relating to colleagues and associates both inside and outside the organization control approach to work.
Ø Ability to work effectively in a multi-cultural context as a good team member.
Ø Good ability to apply statistical methods and data analysis
Ø Expert in preparation of Data submission and Data Anonymization
Ø Ability to develop and maintain R packages or R shiny APP 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, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!