About the job
Job Opportunity As a Senior Statistical Programmer, you will play a pivotal role in supporting end-to-end clinical programming activities across multiple studies. Key responsibilities include programming, validating, and maintaining clinical trial datasets and outputs using SAS and R. • Lead and execute full spectrum of statistical programming deliverables, including creation and review of SDTM and ADaM specifications. • Develop and enhance macros to support study and project requirements. • Work independently with minimal oversight, ensuring timely and high-quality deliverables. We seek an individual with a strong sense of ownership and accountability for assigned tasks, who has proven experience working on oncology clinical trials and possesses a thorough understanding of oncology-specific endpoints and data structures. The ideal candidate has experience mentoring or providing technical oversight to junior programmers and can manage multiple studies simultaneously.
Requirements
- statistical programming
- SAS
- R
- clinical trials
- oncology
Preferred Technologies
- statistical programming
- SAS
- R
- clinical trials
- oncology
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