R&D Programmer III

The Senior Clinical Programmer is responsible to provide high level skills of clinical programming support of clinical projects and regulatory submissions. The Senior Clinical Programmer is playing a lead role generating and validating analysis datasets, tables, listings and figures. The Senior Clinical Programmer participates in the development of global data standards, SDTM, ADaM and Teva s database structure. The Senior Clinical Programmer is responsible for providing professional expertise and leadership through leading departmental tasks and taking initiatives in improving clinical programming processes with focus on SAS Programming.

• Primarily work at the project level
• Provides input for budget planning
• Delivers assignments with quality and within timelines
• May oversee contingent workers and/or vendors; may provide training to others as needed
• Leads/co-leads clinical programming for a study or for a study or for a regulatory submission
• Develops, reviews, documents and performs validation of generic SAS macros
• Initiates and leads new processes, new methodologies and operational ideas; challenge existing ones to improve the effectiveness and efficiency of services provided
• Supervises and supports outsourcing activities

• Bachelor s Degree/master s degree/PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
• Bachelor s Degree +3 years or master s degree +2 years in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
• Experience in SDTM and ADaM acquainted with CDISC Guidelines and requirements.