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, MedDRA, WHO Drug, CTCAE etc.
- Good verbal and written communication
- Demonstrate ability to provide coaching, mentoring, and training to new hires and less-experienced colleagues.
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