We are seeking a skilled Lead Statistical Programmer with expertise in SAS and R programming to support clinical trial data analysis and regulatory submissions.
Key Responsibilities :
- SAS Program Development
- R Programming Expertise
- Data Creation and Analysis
- Cross-Platform Data Transfer
Qualifications & Skills :
Bachelor's or Master's degree in Statistics, Computer Science, Life Sciences, or a related field.Proven experience in SAS programming within clinical trials or pharmaceutical settings.Strong hands-on experience with R programming and relevant packages.Familiarity with CDISC standards (ADAM, SDTM) and regulatory submission requirements.Award-winning opportunities for growth and development await the ideal candidate!