Job Description :
We are seeking an experienced Senior Statistical Programmer to join our team. As a key member of our organization, you will be responsible for performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS / ISE), utilizing SAS programming.
Responsibilities :
- Data manipulation, analysis and reporting of clinical trial data
- Generating and validating SDTM and ADaM datasets / analysis files, and tables, listings, and figures (TLFs)
- Production and QC / validation programming
- Generating complex ad-hoc reports utilizing raw data
- Efficacy analysis
- Creating and reviewing submission documents and eCRTs
- Communicating with internal cross-functional teams and clients for project specifications, status, issues or inquiries
- Lead duties when called upon
Qualifications :
Bachelor's degree in Statistics, Computer Science, Mathematics or related fieldAt least 8 years of SAS programming experience working with clinical trial data in the Pharmaceutical & Biotech industryStudy lead experience, preferably juggling multiple projects simultaneouslySolid understanding of CDISC standards (SDTM & ADaM)Strong analytical and troubleshooting skillsWhat We Offer :
Competitive compensation packageOngoing training and development opportunitiesCollaborative and dynamic work environmentAbout Us :
We are a leading provider of innovative solutions for the pharmaceutical and biotech industries. Our mission is to deliver high-quality results that meet the needs of our clients. If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply.