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3 дня назад

Clinical Trial Assistant (1 Year Contract)

Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
Australia
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Clinical Trial Assistant (1 Year Contract) (Clinical Research): Maintaining clinical trial documentation, Trial Master Files, study records, supplies, Case Report Forms, and clinical data flow with an accent on regulatory accuracy, document completeness, and project timelines. Focus on coordinating clinical communications, supporting CRAs and Regulatory and Start-Up teams, and assisting with site monitoring activities after required training.

Location: North Sydney, New South Wales, Australia

Company

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

What you will do

  • Maintain clinical documents and systems, including Trial Master Files, to track site compliance and performance.
  • Prepare, distribute, file, and archive clinical documentation and reports according to procedures.
  • Review study files for completeness and maintain tracking information for clinical trial supplies.
  • Coordinate Case Report Forms, queries, and clinical data flow.
  • Act as a central contact for project communications, correspondence, and related documentation.
  • Support CRAs during site visits and clinical monitoring activities after completing required training.

Requirements

  • High school diploma or equivalent, with at least one year of administrative support experience.
  • At least one year of clinical research experience is strongly preferred.
  • Working knowledge of Microsoft Word, Excel, and PowerPoint.
  • Good written and verbal English communication skills are required.
  • Effective time management, organizational skills, and the ability to maintain working relationships with colleagues, managers, and clients.
  • Basic knowledge of GCP, ICH guidelines, and applicable clinical research protocol requirements.

Culture & Benefits

  • Full-time employment on a one-year contract.
  • Contract renewal or conversion depends on business needs.
  • Work alongside Clinical Research Associates and Regulatory and Start-Up teams.

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