Senior Clinical Programmer: SDTM, Data Modeling & Reporting

Johnson & Johnson; High Wycombe; On-site; GBP 65,000 - 90,000; Full time

Job summary

Johnson & Johnson in the United Kingdom seeks an Experienced Clinical Programmer to lead data management and SDTM submission activities for complex trials. You will develop data models, mappings, and edit checks to support safety, risk, and compliance.

The role requires SAS programming and CDISC SDTM knowledge, with collaboration across cross-functional teams to ensure high-quality data and regulatory readiness.

Qualifications

• Experience in clinical trial programming and data management.
• Experience with SDTM and CDISC submission packages.
• Strong SAS programming skills.
• Ability to translate study requirements into data specifications.

Responsibilities

• Oversee one or more programming activities of moderate to high complexity.
• Review project requirements and identify gaps, propose solutions.
• Ensure latest standards and technologies are used.
• Create specifications for data mapping and submission-ready SDTM packages.
• Lead quality checks and study-specific reports for stakeholders.

Skills

SAS Programming

CDISC SDTM

Data Modeling

Clinical Trial Data Management

Regulatory Compliance

Job description

Johnson & Johnson in the United Kingdom seeks an Experienced Clinical Programmer to lead data management and SDTM submission activities for complex trials. You will develop data models, mappings, and edit checks to support safety, risk, and compliance.

The role requires SAS programming and CDISC SDTM knowledge, with collaboration across cross-functional teams to ensure high-quality data and regulatory readiness.