Senior Statistical Programmer — Regulatory SAS Expert

Biopharma Careers; Uxbridge; Hybrid; GBP 70,000 - 100,000; Full time

Job summary

Bristol Myers Squibb in Uxbridge, UK is seeking a Senior Statistical Programmer to shape data for regulatory submissions and inform decision-making.

You will own programming tasks within GBDS, collaborate with cross-functional teams and external vendors, and deliver high-quality analyses with autonomy.

The role offers hybrid work with 50% onsite and opportunities to impact global medicines.

Qualifications

• Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences.
• Demonstrated industry experience in statistical programming.
• SAS experience to produce Datasets and TFLs; familiarity with SDTM/ADaM.

Responsibilities

• Write and validate SAS programs to generate derived analysis datasets and TFLs used in regulatory submissions.
• Assist with electronic submissions (NDA, BLA, MAA) and regulatory milestones.
• Review SAPs and Data Presentation Plans to guide programming work.
• Collaborate with vendors on standards and file transfers.
• Independently lead programming tasks across multiple projects with minimal supervision.

Skills

SAS proficiency

CDISC SDTM/ADaM

Clinical data standards

Regulatory knowledge

Team collaboration

Analytical thinking

Education

Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences

Tools

Pinnacle 21

XML

MS Office

Job description

Bristol Myers Squibb in Uxbridge, UK is seeking a Senior Statistical Programmer to shape data for regulatory submissions and inform decision-making.

You will own programming tasks within GBDS, collaborate with cross-functional teams and external vendors, and deliver high-quality analyses with autonomy.

The role offers hybrid work with 50% onsite and opportunities to impact global medicines.