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:
Provide high quality and advanced programming support according to global project strategies.
KEY ACCOUNTABILITIES:
Ø Mentor junior programmer
Ø Contribute working groups and initiatives e.g. for the development and testing of department tools.
Ø Review and provide feedback on study documents as per SOPs and RACI requirments.
Ø Project oriented
· In cooperation with SB and PPL, plan and timely provide high quality statistical programming deliverables following department SOP’s and guidelines.
· In cooperation with the SB provide the programming specifications for the analysis datasets for a study and implement study metadata.
· Perform programming activities for statistical deliverables
· Perform quality control, as required per SOPs, for statistical programming deliverables (including input in Validation Plan & QC documentation)
· Perform advanced ad-hoc and explortary analysis as requested.
· Prepare project specific items required for e-submission including SDTM, ADaM, TLG, BIMO packages etc.
Ø Standard operation oriented
· In cooperation with SP/SB/PPL, plan and timely provide high quality centrailized standard programming deliverables utilizing department standard tools and following department SOP’s and guidelines.
· In cooperation with the SP/SB, provide the centrailized standard programming specifications (including SDTM and ADaM) for a study and implement study metadata.
· Perform centrailized standard programming activities for statistical deliverables.
· Perform quality control, as required per SOPs, for centrailized standard programming deliverables (including input in Validation Plan & QC documentation).
· Prepare standard items required for e-submission, including aCRF, SDTM, ADaM, TLG, BIMO packages.
JOB-HOLDER ENTRY REQUIREMENTS:
Education:
Bachelor or master degree in statistics, computer science, or relevant filed
Experience & knowledge:
Ø At least 5 year working experience in clinical trial development
Ø Ability to support study requirements with challenging timelines under direct supervision by the PPL/PTAH.
Ø Good SAS programming skill required
Ø Experience in R and/or python preferred.
Core competencies:
Ø 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.
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!