Senior Statistical Programmer

September 16, 2026
Application ends: December 15, 2026
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Job Description

Responsibilities

Technical:

  • Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs
  • Author and review simple and complex study TFL shells
  • Author and review simple and complex dataset standards
  • Perform data checks and data exploration (e.g. using frequencies, histograms)
  • Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice
  • Complete and review CDISC Validation tool reports
  • Ensure the appropriate standards are being applied and adhered to
  • Familiarization with simple statistical techniques (e.g. t-test, ANOVA, regression, standard survival)
  • Review of project management related documents
  • Maintain study master file documents and any other documents that are required to be audit ready

General:

  • Lead internal and client study team meetings effectively
  • Present study updates internally and at client meetings
  • Share scientific, technical and practical knowledge within the team and with colleagues
  • Perform work in full compliance with applicable legislation, regulations, company policies, procedures, and training
  • Build effective collaborative working relationships with internal and client team members
  • Seek opportunities to develop innovative ideas, sharing when appropriate
  • Line management or mentorship of more junior team members
  • Contribution to development of internal training materials
  • Contribution to internal process improvement initiatives

Qualifications

  • Degree in a relevant field such as Mathematics, Life Sciences, Statistics, Computer Science, etc.
  • At least 5+ years of relevant industry experience

Required Skills

  • Understanding of clinical drug development process, relevant disease areas, endpoints and study designs
  • Strong SAS programming skills with SDTM, ADaM, and TFL development experience
  • Good knowledge of CDISC standards and clinical trial processes
  • Experience reviewing protocols, SAPs, CRFs, and CSR documents
  • Hands on experience in R Programming.
  • Proficiency in data handling using SAS or other statistical software (e.g. R)
  • Awareness of industry and project standards & ICH guidelines
  • Demonstrated problem solving ability and attention to detail
  • Ability to work independently and as part of a team
  • Excellent verbal and written communication skills
  • Interpersonal/teamwork skills for effective interactions
  • Self-management skills with a focus on results for timely and accurate completion of competing deliverables

Are you interested in this position?
Apply by clicking on the “Apply Now” button below!
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