Назад
Company hidden
7 дней назад

Senior Statistical Programmer/Analyst Consultant (Clinical Programming)

Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Senior Statistical Programmer/Analyst Consultant (Clinical Programming): Supporting statistical programming deliveries for clinical studies and development programs with an accent on CDISC, regulatory standards, documentation, and deliverable quality. Focus on independently implementing protocol programming, coordinating with study teams, automating compliant processes, and managing risks across concurrent project activities.

Location: Remote in the United States

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

  • Support statistical programming deliveries for clinical studies and projects.
  • Implement programming aspects of clinical protocols and development programs.
  • Program independently while maintaining high efficiency, quality, and compliance.
  • Write or implement specifications and oversee relevant documentation.
  • Plan and support team activities, contribute to best practices, and promote automation.
  • Communicate and escalate project risks while collaborating with statisticians, lead programmers, data managers, and study leaders.

Requirements

  • Bachelor’s degree in computer science, statistics, or a related scientific discipline with 5 years of clinical programming experience, including CDISC; or a master’s degree with 6 years of experience.
  • Working knowledge of ICH, Good Clinical Practices, clinical research, clinical trial processes, and regulatory terminology.
  • Strong understanding of the clinical drug development process.
  • Strong communication, coordination, stakeholder-influencing, and concurrent activity management skills.
  • Must be based in the United States for this remote role.

Culture & Benefits

  • Work directly with a single sponsor while receiving the security and career opportunities of a global CRO.
  • Client-facing environment with independent work and high-trust collaboration.
  • Continuous training and professional development focused on maintaining technical and functional expertise.
  • Supportive, diverse, and inclusive workplace culture.
  • Equal opportunity employment environment.

Hiring process

  • Submit a CV and receive an application acknowledgement.
  • Qualified candidates are invited to a phone interview as the first step.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →