Biostatistical Programming Senior Associate

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a results-oriented, tech-forward programming leader with deep expertise in clinical trial operations and digital transformation.

Basic Qualifications :

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects, with at least 4 years of statistical programming experience in relevant career statistical programming experience in a clinical development environment.

Familiarity with drug development life cycle and excellent skills with the manipulation, analysis and reporting of complex clinical trial data

Ability to effectively perform complex statistical programming and related tasks

Ability to provide quality output and deliverables in adherence with challenging timelines

Ability to work effectively on multiple tasks or projects across therapeutic areas

Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners

Working knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards with strong ability to implement the standards

In depth knowledge of SAS/STAT packages

Familiar with data quality and compliance check tools

Excellent oral and written English communication skills

Preferred Skills :

MSc or higher degree in statistics, biostatistics, mathematics, or related quantitative or scientific subjects

Familiarity with open-source programming tools (R, Python), automation platforms, and emerging technologies in statistical programming

Prior regulatory submission experience for drug approval