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6 дней назад

Senior Statistical Programmer/Analyst Consultant (Hybrid at NJ/PA)

Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Senior Statistical Programmer/Analyst Consultant (Clinical Programming): Supporting statistical programming deliveries for clinical studies and development programs with an accent on CDISC standards, regulatory requirements, and high-quality documentation. Focus on independently programming study deliverables, implementing specifications, coordinating with statisticians and data managers, and managing concurrent project risks.

Location: United States; hybrid at NJ/PA

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 programming deliveries for clinical studies and projects.
  • Implement statistical programming aspects of protocols and clinical development programs.
  • Program independently while ensuring high efficiency and quality in personal and team deliverables.
  • Write and implement specifications, oversee relevant documentation, and ensure compliance with standards and automation usage.
  • Plan and support team activities, communicate and escalate study or project risks, and contribute to programming best practices.
  • Work proactively with statisticians, lead programmers, data managers, study leaders, and other study team members.

Requirements

  • Bachelor’s degree in computer science, statistics, or a related scientific discipline with 5 years of clinical programming experience in CDISC; or a master’s degree in a related discipline with 6 years of clinical programming experience in CDISC.
  • Working knowledge of ICH, Good Clinical Practices, clinical research, clinical trial processes, and related regulatory requirements and terminology.
  • Good understanding of the clinical drug development process.
  • Strong communication and coordination skills.
  • Current knowledge of technical and regulatory requirements relevant to the role.
  • Ability to proactively manage concurrent project activities.
  • Ability to influence relevant stakeholders on programming-related matters.

Culture & Benefits

  • Hybrid work arrangement at NJ/PA.
  • Client-facing work with the security and career opportunities of a global CRO.
  • Supportive culture focused on quality and professional development.
  • Continuous training to maintain technical and process expertise.
  • Work within a diverse and inclusive equal opportunity organization.

Hiring process

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

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