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Protocol Intelligence
Data-driven signals on your job's competitivenessMetro, mid-level role with Sanofi association, but niche SAS/CDISC skills limit applicant density.
Clinical trial SAS and CDISC expertise makes skills poorly transferable outside pharma/regulatory contexts.
Explicit minimum experience and mandatory SAS plus CDISC SDTM/ADaM requirements enforce strict screening.
Job Description
Structured overview of role & requirementsAbout This Role
Implement statistical analysis plans and produce QC’d data packages (tables, figures, listings) for publications and ad-hoc analyses.
Develop, implement, and document advanced statistical programming techniques and non-routine macros in SAS.
Ensure SOP compliance while meeting project timelines and quality standards and collaborate closely with Medical Affairs biostatisticians and programming teams.
Minimum Requirements
Minimum 4 years of relevant experience with Master's degree or minimum 6 years with B.Sc.
Advanced SAS programming skills mandatory.
Familiarity with CDISC standards SDTM & ADaM required.
Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field.
Ideal Candidate Profile
Experienced in clinical trial data analysis in a biostatistics or medical affairs environment, interfacing with global medical stakeholders.
Able to produce well-documented, high-quality data packages under timelines.
Capable of independently handling advanced statistical programming tasks and managing stakeholder expectations effectively.