Principal SAS Programmer & Clinical Trials Lead

Clinvia; San Francisco (CA); On-site; USD 120,000 - 160,000; Full time

Job summary

Clinvia is seeking a Principal Statistical Programmer to lead data analysis and contribute to statistical analysis plans. This position requires a strong background in SAS programming and at least 8 years of experience in the Pharmaceutical/Biotech sector.

The role will involve creating CDISC SDTM and ADaM files, as well as ensuring data quality and compliance for NDA submissions. Candidates should have a BS/MS in Statistics or a related field.

Qualifications

• Minimum 8 years Pharmaceutical/Biotech programming experience.
• NDA submission experience and knowledge required.
• Strong SAS programming and Statistical background.

Responsibilities

• Lead project level activities and perform data analysis.
• Create CDISC SDTM and ADaM files for electronic submissions.
• Contribute to statistical analysis plans and collaborate with clinical teams.

Skills

SAS programming

Statistical analysis

Data analysis

Education

BS/MS in Statistics, Math or Scientific Discipline

Tools

SAS Base

SAS/Macros

SAS/Graph

SAS/Stat

Job description

Clinvia is seeking a Principal Statistical Programmer to lead data analysis and contribute to statistical analysis plans. This position requires a strong background in SAS programming and at least 8 years of experience in the Pharmaceutical/Biotech sector.

The role will involve creating CDISC SDTM and ADaM files, as well as ensuring data quality and compliance for NDA submissions. Candidates should have a BS/MS in Statistics or a related field.