Senior SAS Programmer: SDTM/ADaM Lead, Remote

Cytel (EMEA); Remote; GBP 60,000 - 80,000; Full time

Job summary

A pharmaceutical consulting firm is looking for a Senior Statistical Programmer to support Phase I-IV clinical trials. The role demands advanced SAS programming skills and expertise in CDISC standards. Responsibilities include analyzing clinical trial data, generating datasets, and creating detailed reports. Ideal candidates should have at least 8 years of experience in the Pharma/Biotech sector, strong analytical capabilities, and the ability to thrive in a dynamic team environment. This position offers the flexibility of remote work.

Benefits

Collaborative work environment

Autonomy in role

Support of a dedicated client team

Qualifications

• 8+ years of SAS programming experience in clinical trials within Pharma/Biotech.
• Experience implementing CDISC SDTM/ADaM standards.
• Ability to manage multiple studies simultaneously.

Responsibilities

• Perform data manipulation, analysis, and reporting of clinical trial data.
• Generate and validate SDTM and ADaM datasets.
• Create and QC submission documents.

Skills

SAS programming

CDISC standards

Data manipulation and reporting

Efficacy analysis

Validation skills

Ad-hoc reporting

Analytical skills

Education

Bachelor's degree in Statistics, Computer Science, Mathematics

Job description

A pharmaceutical consulting firm is looking for a Senior Statistical Programmer to support Phase I-IV clinical trials. The role demands advanced SAS programming skills and expertise in CDISC standards. Responsibilities include analyzing clinical trial data, generating datasets, and creating detailed reports. Ideal candidates should have at least 8 years of experience in the Pharma/Biotech sector, strong analytical capabilities, and the ability to thrive in a dynamic team environment. This position offers the flexibility of remote work.