Senior SDTM Statistical Programmer – Lead Data Strategy

Bristol-Myers Squibb Co; Uxbridge; Hybrid; GBP 65,000 - 90,000; Full time

Job summary

Bristol Myers Squibb in the UK is seeking a Senior SDTM Statistical Programmer to lead SDTM strategies across studies and regulatory submissions. You will own technical aspects from protocol review to global filing, mentoring teammates and guiding CRO activities.

This role sits in a hybrid model with 50% onsite work in Uxbridge and collaboration across cross-functional study teams. You will apply strong SAS programs, experience with CDISC/SDTM, and a record of delivering quality outputs that

Qualifications

• 4+ years of pharmaceutical or CRO experience as a SAS Programmer supporting clinical trials and regulatory submissions.
• Deep expertise in CDISC/SDTM standards and a thorough understanding of the clinical development lifecycle.
• Exceptional SAS programming skills (Base, Stat, Graph) and comfort working across complex, multi-source data environments.

Responsibilities

• Own SDTM strategies from protocol review through global regulatory submission.
• Serve as the technical lead on assigned studies and mentor team members.
• Provide guidance and quality oversight to CRO and vendor programming activities.

Skills

SAS programming

CDISC/SDTM standards

Cross-functional collaboration

Leadership

Regulatory submissions

Education

BA/BS or above

Job description

Bristol Myers Squibb in the UK is seeking a Senior SDTM Statistical Programmer to lead SDTM strategies across studies and regulatory submissions. You will own technical aspects from protocol review to global filing, mentoring teammates and guiding CRO activities.

This role sits in a hybrid model with 50% onsite work in Uxbridge and collaboration across cross-functional study teams. You will apply strong SAS programs, experience with CDISC/SDTM, and a record of delivering quality outputs that