The Senior Biostatistician will work with Medical Affairs biostatisticians and MedHub biostatistics and programming personnel to implement statistical analysis plans and provide QC’d data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, and manuscripts)
The Senior Biostatistician will ensure SOPs are followed and timelines and quality metrics are met
Local biostatistics and programming teams
Global Medical Affairs biostatisticians
Global Medical Affairs Scientific Communications personnel
Duties & Responsibilities
Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and programming team members within the allocated Global business unit and product – with an objective to develop statistical data outputs.
Conduct appropriate post-hoc statistical analyses of clinical trial data
Design, develop, test, implement, and document statistical programming in high-level software packages e.g. SAS
Produce well documented data packages that include tables, listings, and figures
Work closely with the Lead Biostatistician and Lead Programmer to develop and implement project QC plans and timelines.
Review appropriate biomedical and clinical research literature related to assigned project(s)
Work closely with Global Medical Affairs biostatisticians to identify statistical analysis needs and assist in developing assigned deliverables
Knowledge, Skills & Competencies / Language
Ability to work independently and within a team environment
Advanced knowledge of SAS statistical procedures
Excellent English language knowledge – written and spoken
Master's degree/Ph.D. in biostatistics or statistics or epidemiology and 2-4 years (Ph.D.)/6-8 years (M.Sc.) of experience required
Requirements of the job
Pharmaceutical/healthcare industry exposure
High proficiency in statistical methods used in the pharmaceutical industry
Advanced SAS and other statistical computing software skills in a clinical data environment across multiple therapeutic areas
Expertise in the use of data management applications and database/file structures, specifically with respect to CDISC requirements
Autonomy in the management of activities; ability to manage multiple conflicting high priority deadlines
Capacity to respond to unscheduled changes in project workload
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.
Please note you are leaving the corporate site of Sanofi and are being redirected to our applicant tracking system, Workday, which allows you to apply to our open positions.