Назад
Company hidden
5 дней назад

Clinical Research Associate Trainee Program (Adelaide)

Формат работы
onsite
Тип работы
fulltime
Грейд
trainee
Английский
b2
Страна
Australia
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 Research Associate Trainee Program (Adelaide) (Clinical Research): Building practical capability in clinical trial monitoring through structured training and supervised site visits with an accent on ICH-GCP, Australian regulatory requirements, and study documentation. Focus on learning site selection, initiation, monitoring, and close-out, tracking study progress, and maintaining Trial Master Files and Investigator Site Files.

Location: Adelaide, Australia; full current Australian work rights required. The role includes supervised site monitoring visits and in-person interviews at hirify.global offices.

Company

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

What you will do

  • Complete a full-time trainee program covering all aspects of clinical trial monitoring.
  • Learn and apply ICH-GCP guidelines and Australian ethical and regulatory requirements.
  • Conduct supervised site selection, initiation, monitoring, and close-out visits.
  • Track regulatory submissions, recruitment, study progress, and data completion.
  • Maintain Trial Master Files and Investigator Site Files.
  • Collaborate with study teams, clinical sites, and colleagues.

Requirements

  • Bachelor’s degree in a healthcare or life-science field, or equivalent experience.
  • Basic understanding of ICH-GCP and Australian clinical research requirements.
  • Full current work rights in Australia are required; visa sponsorship is not available now or in the future.
  • Excellent written and verbal English communication skills.
  • Proficiency in MS Office Suite.
  • Strong problem-solving, critical-thinking, time-management, and relationship-building skills.

Nice to have

  • Prior clinical research experience, such as In-house CRA, CTA, or CRC experience.

Culture & Benefits

  • Modular training combining virtual learning, web-based scenarios, learning clinics, and on-the-job experience.
  • Mentorship from experienced CRAs, Line Managers, and Quality Managers.
  • Continuous evaluation and development through the Train, Transfer, and Sustain approach.
  • Potential progression into CRA, Senior CRA, Clinical Project Manager, or Line Manager roles after successful program completion.

Hiring process

  • Complete a pre-recorded video interview between 15 and 23 October 2026.
  • Attend an in-person assessment interview if selected; assessment-day notifications are expected during the week of 2 November 2026.
  • In-person interviews take place during the week of 16 November 2026, with the program starting on 1 February 2027.

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 →