About this role

Provides leadership, resource planning and coordinating deliverables within project or across multiple projects
Lead programming support for processing/analyzing/storing data from clinical studies according to a Statistical Analysis Plan
Work independently to design and test program logic
Address administrative functions required for project management
Create, manage and maintain the programming specifications for the analysis datasets
Provide programming support for all PMX deliverables

Master in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline
10+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry
Expert SAS programming skills (SAS (Base, Stat, Macro, graph) in a clinical data environment
Strong Experience/knowledge with implementing standardization methodology, creation of current CDISC data standards
Comprehensive understanding of biostatistics, pharmaceutical clinical development (i.e. safety deliverables, efficacy analysis)
Good Skilled in use of relevant software, including Window SAS, SAS studio (Base, Stat, Macro, graph), MS-Excel, R programming and/or Python

health and wellness programs (including medical, dental, vision, life, and disability insurance)
fitness centers
401(k) company match
family support benefits
equity awards
annual bonuses
paid time off
paid leaves (e.g., military and parental leave) for eligible employees at all levels

Associate Director, Statistical Programming – Pharmacometrics

Key skills