Senior Statistical Programming Analyst — On-Site Irvine

Edwards Lifesciences Gruppe; Redhill; On-site; GBP 88,000 - 125,000; Full time

Job summary

Edwards Lifesciences is seeking a Statistical Programmer to drive critical analyses for clinical reports and presentations. You will develop complex datasets and outputs while ensuring regulatory compliance across modeling and reporting tasks.

This on-site role requires a strong background in statistics and SAS, with a move toward collaborating with the Clinical Data Management team to review CRFs and specifications. California-based, on-site location.

Qualifications

• Bachelor's degree in statistics, mathematics, CS or related field required.
• 4 years of statistical programming experience (SAS) required.
• Master's degree or equivalent in statistics, mathematics, CS or related field required.
• 2 years of statistical programming experience (SAS) preferred when applicable.

Responsibilities

• Plan the execution of programs in statistical programming languages within project.
• Develop complex analysis datasets, specifications, and summary output for clinical reports or presentations.
• Create complex programs that meet regulatory and company standards for efficient programming and reporting.
• Review and validate statistical programs to meet regulatory and company standards.
• Perform complex analysis in response to data requests with designated statistician.
• Collaborate with CDM and statistician to review draft CRFs, database specifications, and edit checks.

Skills

Statistical programming experience

MS Office integration with SAS

Education

Bachelor's Degree in Statistics, Mathematics, Computer Science or related field

Master's Degree or equivalent in Statistics, Mathematics, Computer Science or related field

Tools

SAS

Job description

Edwards Lifesciences is seeking a Statistical Programmer to drive critical analyses for clinical reports and presentations. You will develop complex datasets and outputs while ensuring regulatory compliance across modeling and reporting tasks.

This on-site role requires a strong background in statistics and SAS, with a move toward collaborating with the Clinical Data Management team to review CRFs and specifications. California-based, on-site location.