Senior Statistical Programmer/Analyst Consultant (Hybrid at NJ/PA)
Контакты
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
regulatory compliancesasclinical trialscdiscclinical programmingstatistical programmingichgood clinical practice
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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У старшей роли понятные задачи в клиническом программировании и четкий регуляторный контекст, но работа в CRO может означать смену проектов и команд, а также меньше стабильности, чем в продуктовой компании.
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Актуальный инструментарийПонятные задачиРабота в CRO
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
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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