Senior Programmer – Clinical Study

CSL

Senior Programmer designing and validating clinical study deliverables for CSL Behring. Collaborating with statisticians and teams to ensure timely and accurate clinical data output.

Posted 5/5/2026full-timeKing of Prussia • Massachusetts, Pennsylvania • 🇺🇸 United StatesSeniorWebsite

About the role

Key responsibilities & impact

Collaborates with the study statistician to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, Tables, Figures, Listings and Analysis Submission content
Leads the production and validation efforts for the designed output, this may include oversight of work by CROs
Collaborates with peers and statisticians to ensure the quality and accuracy –thus submission readiness –of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml)
Supports the review of related deliverables when provided by CROs
Leads requested efforts for pooled and exploratory analyses working closely with clinical programming team and their collection of legacy data
Leads the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO
Leads the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format
Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group
Works closely with clinical study teams to ensure that project timelines are met with high quality deliverables

Requirements

What you’ll need

BSc in Computer Science, Mathematics, Statistics or related area with relevant experience
At least 5 years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software
Understanding of clinical programming and/or statistical programming processes and standards
Experiences with statistical programming using the SAS software including development and use of SAS Macros
Knowledge in CDISC standards (CDASH, SDTM, ADaM)
Ability to work effectively in a team setting, and to meet set goals by managing own timelines
Ability to work in cross-functional, multicultural and international clinical trial teams
Good communication and analytical skills
Good planning and organizational skills
Ability to work successfully in a matrix organizational structure
Networking skills and ability to share knowledge and experience amongst colleagues
Fluent in English, oral and in writing.

Benefits

Comp & perks

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL

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Hard Skills & Tools

SASSAS MacrosADaMSDTMCDISCstatistical programmingclinical programmingdata structure designdata validationdata analysis

Soft Skills

teamworkcommunicationanalytical skillsplanningorganizational skillsproblem-solvingnetworkingcross-functional collaborationtime managementmulticultural teamwork