Назад
Company hidden
8 дней назад

Clinical Trial Assistant 2 (Clinical Research)

Формат работы
hybrid
Тип работы
fulltime
Грейд
junior
Английский
c1
Страна
Netherlands
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
Clinical Trial Assistant 2 (Clinical Research): Supporting clinical teams with study documentation, clinical systems, trial supplies, case report forms, and project communications with an accent on regulatory compliance, data flow, and trial file quality. Focus on maintaining study records, coordinating clinical documentation and supplies, and supporting monitoring activities under GCP and ICH requirements.

Location: Amsterdam, Netherlands; must be based in the Netherlands. Regular travel to the Breda office is required, typically two days per week.

Company

hirify.global provides contract research services, advanced analytics, technology solutions, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Maintain clinical systems tracking site compliance and performance within project timelines.
  • Prepare, distribute, file, archive, and review clinical documentation and study reports.
  • Support the preparation and tracking of clinical trial supplies.
  • Track Case Report Forms, queries, and clinical data flow.
  • Coordinate project communications and documentation for the clinical team.
  • Support CRAs during site visits and perform administrative tasks related to clinical trial execution after required training and approval.

Requirements

  • Must be based in the Netherlands and travel regularly to the Breda office, typically two days per week.
  • At least one year of Clinical Trial Assistant experience.
  • Fluent written and verbal English and Dutch.
  • Strong understanding of Good Clinical Practice and International Conference on Harmonization guidelines.
  • Knowledge of applicable clinical trial protocol requirements.
  • Working knowledge of Microsoft Word, Excel, and PowerPoint, together with strong organizational and communication skills.

Culture & Benefits

  • Work within a full-service clinical research model and a specific therapeutic area.
  • Access to technology developed for Clinical Trial Assistants.
  • World-class training and professional development opportunities.
  • Inclusive and respectful workplace culture focused on diversity, belonging, and personal development.

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 →