Manager, Statistical Programming

Rezolute

• $160K — $195K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • BS/BA in Statistics, Computer Science, Mathematics, Life Sciences, or related field; MS preferred.
  • 8+ years of statistical programming experience in pharma, biotech, or CRO with a BS, or 6+ years with an MS.
  • 1-2 years of experience supervising programmers or serving as lead programmer on a study.
  • Strong SAS skills (Base, Macro, SQL, STAT, ODS/Graph).
  • Working proficiency in R for clinical data manipulation, analysis, and reporting.
  • Experience developing R Shiny applications for interactive data review is a plus.
  • Familiarity with ICH guidelines and GCP; exposure to regulatory submissions is a plus.

Responsibilities

  • Plans and delivers statistical programming for clinical trials and regulatory submissions.
  • Tracks programming timelines and flags risks to ensure alignment with study schedules.
  • Creates and oversees CDISC-compliant SDTM and ADaM datasets, performing conformance checks before delivery.
  • Develops and validates TLFs and analysis datasets using SAS and R; conducts independent QC of programming.
  • Assigns and reviews work of internal and CRO programmers, providing direction and mentoring.
  • Reviews CRO deliverables for quality and standards compliance, escalating issues as needed.
  • Participates in study meetings to develop specifications and reports.

Benefits

  • Health Insurance (Medical / Dental / Vision)
  • Disability, Life & Long-Term Care Insurance
  • Holiday Pay
  • Tracking Free Vacation Program
  • 401(k) Plan Match
  • Educational Assistance Benefit
  • Fitness Center Reimbursement
Full Job Description
The Manager of Statistical Programming is responsible for delivering study-level programming deliverables and milestones. The role combines hands-on programming in SAS and R with oversight of a small team or of CRO programmers assigned to a study.

The position requires working knowledge of statistical programming languages and software, clinical trial data, and the drug development process. The incumbent develops and oversees programs that generate CDISC-compliant SDTM and ADaM datasets, TLFs, and reports supporting the review of clinical data. The incumbent also writes validation programs and general-purpose code, prepares documentation to support electronic submissions, and contributes to programming standards and templates.

Responsibilities

  • Plans and delivers statistical programming for assigned studies in support of clinical trials, regulatory submissions, publications, and ad hoc analysis requests, following applicable regulatory guidelines and standards.
  • Tracks programming timelines for assigned studies and flags risks to the Director so deliverables stay aligned with the study schedule.
  • Creates or oversees the creation of CDISC-compliant SDTM and ADaM datasets, and performs conformance checks (e.g., Pinnacle 21) before delivery.
  • Develops and validates TLFs and analysis datasets using SAS and R; performs independent QC of programming produced by others, including cross-language validation where appropriate.
  • Assigns and reviews the work of a small team of internal programmers and/or CRO programmers; provides day-to-day direction, feedback, and mentoring.
  • Reviews CRO deliverables, specifications, and documentation for quality and standards compliance, and escalates issues as needed.
  • Participates in study meetings with Clinical Operations, Data Management, Safety, and Biostatistics to develop specifications and reports.
  • Writes and maintains batch scripts to schedule SAS and R jobs and distribute reports to the clinical team.
  • Prepares programming documentation supporting electronic submissions, including define.xml inputs and reviewer guide content.
  • Contributes to the development of SAS macros, R functions, standards, templates, and SOPs, and to cross-functional initiatives.
  • Provides input on programming tools and infrastructure needs, including SAS and R environments, and works with IT as needed.


Qualifications

  • BS/BA in Statistics, Computer Science, Mathematics, Life Sciences, or a related field; MS preferred.
  • 8+ years of statistical programming experience in pharma, biotech, or CRO with a BS, or 6+ years with an MS.
  • 1-2 years of experience supervising programmers or serving as lead programmer on a study.
  • Strong SAS skills (Base, Macro, SQL, STAT, ODS/Graph).
  • Working proficiency in R for clinical data manipulation, analysis, and reporting (e.g., tidyverse, admiral, gt, rtables, or similar).
  • Experience developing R Shiny applications for interactive data review, safety monitoring, or visualization of clinical trial data is a plus.
  • Working knowledge of CDISC SDTM and ADaM, controlled terminology, and Define-XML.
  • Familiarity with ICH guidelines and GCP; exposure to a regulatory submission is a plus.
  • Experience with Python for automation, data processing, or tooling is a plus.
  • Clear written and verbal communication; comfortable working directly with statisticians and clinical teams.


Rezolute (RZLT) currently anticipates the base salary for the Manager of Statistical programming role could range from $160,000 to $195,000 and will depend in part on the successful candidate's geographical location and their qualifications for the role, including education and experience. This position will also be eligible for an annual performance bonus in accordance with the terms of the applicable plan (depending, in part, on company and individual performance and at the Company's discretion on an individual basis). The compensation described above is subject to change and could be higher or lower than the range described based on current market survey data and the qualifications, education, experience, and geographical location of the selected candidate.

Qualifying employees are eligible to participate in benefit programs such as:

  • Health Insurance (Medical / Dental / Vision)
  • Disability, Life & Long-Term Care Insurance
  • Holiday Pay
  • Tracking Free Vacation Program
  • 401(k) Plan Match
  • Educational Assistance Benefit
  • Fitness Center Reimbursement


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