Lead Statistical Programmer Opportunity
We are seeking a highly skilled and detail-oriented Lead Statistical Programmer to support clinical trial data analysis and regulatory submissions.
- The ideal candidate will be responsible for authoring, validating, and documenting SAS programs for datasets and macros.
- Strong hands-on experience with R programming and relevant packages such as Tidyverse is required.
- The successful candidate will also create ADaM datasets using Admiral packages in R and conduct thorough debugging using R console tools.
Required Qualifications & Skills :
A Bachelor's or Master's degree in Statistics or Computer Science is essential.Proven experience in SAS programming within clinical trials or pharmaceutical settings is mandatory.Knowledge of CDISC standards (ADaM, SDTM) and regulatory submission requirements is necessary.This role requires a strong communicator with excellent problem-solving skills who can thrive in a fast-paced environment.
Benefits :
Opportunity to work with cutting-edge technologies and innovative projects.Chance to develop and maintain R programs with hands-on experience in relevant packages.What We Offer :
Competitive compensation package.Comprehensive benefits including health insurance, retirement plan, and paid time off.