Senior Manager, Statistical Programming

Immunovant

. Perform programming and statistical analyses necessary to analyze clinical trial and related research results .

Posted 10/15/2026full-timeRemote • North Carolina • United StatesSenior💰 $175,000 - $195,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in SAS programming, statistical analysis, and clinical data reporting, with a strong focus on drug development processes and collaboration with CROs. Proficient in developing and validating statistical programs and outputs in compliance with regulatory standards.

Highest-signal resume keywords

SAS ProgrammingStatistical AnalysisCDISC SDTMClinical Data AnalysisCRO Collaboration

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

SAS ProgrammingStatistical AnalysisStatistical ProgrammingDatabase SystemsStatistical Analysis PlansCDISC SDTMADaMESubmissionStatistical Programming TrainingData Analysis

Soft Skills

Interpersonal SkillsCommunication SkillsOrganizational SkillsAdaptability

Tools & Technologies

SAS/StatSAS/GraphSAS MacrosODS

Industry Keywords

BiotechPharmaceuticalCRONDA SubmissionMAA Submission

About the role

Key responsibilities & impact

Perform programming and statistical analyses necessary to analyze clinical trial and related research results
Contribute to interpretation of analysis results and provide statistical input for reporting
Validate and cross-check external CRO statistical programs and resulting Tables, Listings and Graphs (TLGs)
Participate in development and maintenance of the SAS macro library and safety database
Interact with CROs to ensure analyses and outputs are accurate and consistent with agreed deliverables
Characterize and resolve data analysis issues with vendor staff
Produce statistical analyses according to protocols and Statistical Analysis Plans (SAPs)
Develop statistical programs and outputs for integrated scientific reports
Provide statistical input for SAPs, publications, scientific presentations, and promotional material
Review Case Report Forms (CRFs), CRF annotations, SAPs, TLG shells, and TLGs
Represent statistical programming in study team meetings and communicate statistical issues to development teams
Participate in CRO assessment, selection, and evaluation
Create and review derived dataset specifications and related analysis datasets
Develop statistical programming training guidelines

Requirements

What you’ll need

Master’s degree in a quantitative sciences discipline (e.g., Statistics, Mathematics, Computer Science) and a minimum of 7 years in statistics or statistical programming in a biotech/pharmaceutical or CRO environment
Bachelor’s degree in a quantitative sciences discipline (e.g., Statistics, Mathematics, Computer Science) and a minimum of 10 years in statistics or statistical programming in a biotech/pharmaceutical or CRO environment
Excellent SAS programming skills (e.g., Base SAS, SAS/Stat, SAS/Graph, SAS macros, ODS) and a good understanding of database systems
Experience leading programming activities involving CDISC SDTM, ADaM, and eSubmission (e.g., define.xml, ADRG/SDRG)
Applied knowledge of clinical data analysis and reporting process as it relates to drug development
Excellent interpersonal and communication skills
Good organizational skills with the ability to adapt and adjust to changing priorities
Experience working with CROs
NDA/MAA submission experience

Benefits

Comp & perks

Equity and other forms of compensation may be provided as part of a total compensation package
Medical benefits
Dental benefits
Vision benefits
401k
Unlimited paid time off
Parental leave
Remote work
Dynamic, interactive, fast-paced, and entrepreneurial environment