Senior Statistical Programmer: Clinical Trial Analytics

Edwards Lifesciences Gruppe; Redhill (MS); On-site; USD 119,000 - 168,000; Full time

Job summary

Edwards Lifesciences Gruppe seeks a Statistical Programmer to support clinical data analysis and reporting. You will develop analysis datasets, specifications, and output for submissions using SAS or R, ensuring compliance with regulatory standards.

The role requires a Statistics/Math/CS background with 2–4 years of statistical programming experience, plus strong communication and MS Office integration skills.

Qualifications

• Bachelor’s or Master’s degree in statistics, mathematics, computer science or related field.
• 2–4 years of statistical programming experience with SAS or similar tools.

Responsibilities

• Develop complex analysis datasets, specifications, and summary outputs for clinical reports or presentations.
• Create programs in SAS or R to support data analysis and regulatory submission requirements.
• Review and validate statistical programs and ensure documentation meets regulatory and company standards.

Skills

SAS

Statistics

R

MS Office integration

Education

Bachelor's degree in Statistics/Mathematics/Computer Science

Master's degree in Statistics/Mathematics/Computer Science

Tools

SAS

R

SQL

Job description

Edwards Lifesciences Gruppe seeks a Statistical Programmer to support clinical data analysis and reporting. You will develop analysis datasets, specifications, and output for submissions using SAS or R, ensuring compliance with regulatory standards.

The role requires a Statistics/Math/CS background with 2–4 years of statistical programming experience, plus strong communication and MS Office integration skills.