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The opportunity
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.
How you’ll spend your day
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