Job Description:

 Master’s degree, equivalent, or higher in Biostatistics, mathematics, computing, or related field

 Minimum 8 + years of experience, or an equivalent combination of education or experience to successfully perform the key responsibilities of the job

 Experience with SAS statistical software

Must have experience in SDTM and ADAM and TLF

 Experience leading statistical programming activities in clinical research

 Previous Oncology experience (safety and efficacy) in pharmaceutical research or CRO setting preferred

 Knowledge of one or more statistical software packages (SAS® preferred + R) used to conduct statistical analyses

 Experience with CDISC standards and other industry guidance/dictionaries like RECIST criteria, Med DRA, WHO Drug, CTCAE etc.

 Good verbal and written communication

 Demonstrate ability to provide coaching, mentoring, and training to new hires and less experienced colleagues.