Назад
Company hidden
4 дня назад

ADAM Standards Engineer (SAS/Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
Germany
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
ADAM Standards Engineer (SAS/Clinical Research): Developing and maintaining ADaM metadata programming standards and integrated statistical programming solutions for complex clinical studies with an accent on CDISC ADaM datasets, SAS programming, and data validation. Focus on designing analysis databases, validating data with P21, coordinating statistical programming activities, and leading technical delivery for complex studies.

Location: Frankfurt, Hesse, Germany

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Develop and maintain standard ADaM metadata programming for complex clinical studies.
  • Plan, coordinate, program, test, and document statistical tables, figures, listings, analysis databases, and data transfers.
  • Integrate databases from multiple studies or sources and develop programming documentation, plans, and specifications.
  • Develop, implement, and validate process technologies, macros, and applications.
  • Lead statistical programming delivery for single complex studies or groups of studies.
  • Provide technical consulting, training, and guidance to internal teams, clients, and junior staff while managing scope, resources, and forecasts.

Requirements

  • Master’s and bachelor’s degrees in computer science or a related field.
  • Knowledge of statistics, programming, and clinical drug development processes.
  • Advanced knowledge of Base SAS, SAS Graph, and SAS Macro Language.
  • Strong understanding of CDISC ADaM datasets and experience managing ADaM standards.
  • Hands-on experience with P21 for data validation and basic knowledge of eSubmission documents, including ADRG and Define.
  • Strong organizational, communication, interpersonal, leadership, multitasking, and attention-to-detail skills.

Nice to have

  • Knowledge of tables, listings, and figures.

Culture & Benefits

  • Work in clinical research and healthcare intelligence supporting the development and commercialization of medical treatments.
  • Collaborate with internal and external clients across complex studies and statistical programming projects.
  • Opportunity to provide technical leadership, internal consulting, training, and mentoring.

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 →