Senior Statistical Programming Lead for Clinical Trials

Edwards Lifesciences Gruppe; California (MO); Hybrid; USD 151,000 - 215,000; Full time

Job summary

Edwards Lifesciences seeks a Senior Statistical Programmer to lead clinical studies, oversee a team of programmers, and collaborate with project statisticians. The role demands deep expertise in SAS, SDTM/ADAM/TLF, and regulatory guidelines, with a track record in medical device or pharma settings.

The candidate will ensure programming meet regulatory standards, develop analysis datasets, and contribute to study reports and publications within a cross-functional team in a dynamic environment.

Qualifications

• Bachelor's degree in Statistics, Mathematics, Computer Science or related field with 10 years experience in statistical analysis.

Responsibilities

• Lead on clinical studies and manage a team of statist programmers.

Skills

Project management

SAS

Windows OS

Regulatory knowledge

MS Office

Communication

Leadership

Statistical programming

SDTM/ADAM/TLF/Macros

R/S-Plus

Education

Bachelor's degree in Statistics / Mathematics / Computer Science / related field

Master's degree in a regulated industry

Tools

MS Office suite

Regulatory guidelines experience tools

Job description

Edwards Lifesciences seeks a Senior Statistical Programmer to lead clinical studies, oversee a team of programmers, and collaborate with project statisticians. The role demands deep expertise in SAS, SDTM/ADAM/TLF, and regulatory guidelines, with a track record in medical device or pharma settings.

The candidate will ensure programming meet regulatory standards, develop analysis datasets, and contribute to study reports and publications within a cross-functional team in a dynamic environment.