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5 дней назад

Senior/Principal Statistical Programmer/Analyst Consultant (Cardiovascular, Renal) (SAS)

Формат работы
remote (только United_kingdom)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
UK
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior/Principal Statistical Programmer/Analyst Consultant (Cardiovascular, Renal) (SAS): Developing, validating, and maintaining SAS programs, clinical datasets, tables, listings, and figures for cardiovascular, renal, metabolism, respiratory, and immunology studies with an accent on CDISC-compliant SDTM and ADaM data and TLF production. Focus on supporting clinical trial reporting, collaborating with biostatistics and clinical teams, and delivering high-quality programming for regulatory submissions.

Location: Remote, United Kingdom

Company

hirify.global is a global full-service contract research organization providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

What you will do

  • Develop, validate, and maintain SAS programs for clinical study data analysis and reporting.
  • Create SDTM and ADaM datasets, tables, listings, and figures according to study requirements.
  • Collaborate with Biostatistics, Data Management, Clinical, and client teams.
  • Review specifications, participate in study planning, and support regulatory submission activities.
  • Ensure programming deliverables meet quality standards and project timelines.

Requirements

  • Senior or principal-level experience in clinical statistical programming, including 5 years with a bachelor's degree or 6 years with a master's degree.
  • Strong SAS programming experience in the pharmaceutical or CRO industry.
  • Hands-on experience supporting cardiovascular, renal, and metabolism studies, plus respiratory or immunology therapeutic-area experience.
  • Experience generating and validating SDTM, ADaM, and TLFs, with a good understanding of CDISC standards.
  • Working knowledge of ICH, Good Clinical Practices, clinical research, clinical trial processes, and regulatory terminology.
  • Ability to work independently, manage multiple priorities, and communicate effectively with stakeholders.

Nice to have

  • Experience supporting regulatory submissions.

Culture & Benefits

  • Remote consultant engagement outside IR35.
  • Opportunity to work directly with a single sponsor while receiving the support and career opportunities of a global CRO.
  • Professional development supported through continuous training.
  • Work within a quality-focused and supportive environment.

Hiring process

  • CV submission followed by an acknowledgement of receipt.
  • Phone interview as the first step for candidates meeting the requirements.

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