Deliver results-driven statistical programming solutions for clinical trials, leveraging advanced SAS skills and CDISC standards expertise.
This role offers flexible work arrangements, empowering you to excel in a collaborative environment.
Our core values include applying scientific rigor, fostering intellectual curiosity, collaboration, innovation, and intelligent solutions using cutting-edge technology.
Main Responsibilities :
- Data manipulation, analysis, and reporting for clinical trial data utilizing SAS programming
- Generating and validating SDTM and ADaM datasets / analysis files, tables, listings, and figures
- Production and QC / validation programming
- Complex ad-hoc reports from raw data
- Efficacy analysis application
- Submission documents and eCRTs creation and review
- Communication with internal teams and clients on project specifications, status, issues, or inquiries
Qualifications and Requirements :
Bachelor's degree in Statistics, Computer Science, Mathematics, etc.At least 8 years of SAS programming experienceStudy lead experienceSolid CDISC SDTM / ADaM skillsSubmissions experience utilizing define.xmlKey Skills :
Advanced SAS programming skillsCDISC standards expertiseStatistical programmingData analysisReport generationCommunication skillsWhat We Offer :
Flexible work arrangementsCollaborative environmentOpportunities for growth and development