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8 дней назад

Senior Clinical Trial Assistant (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Thailand
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
Senior Clinical Trial Assistant (Clinical Research): Maintaining Trial Master Files, clinical documentation, trial supplies, Case Report Forms, queries, and clinical data flow with an accent on regulatory compliance, document accuracy, and coordination with CRAs and Regulatory and Start-Up teams. Focus on reviewing study-file completeness, mentoring Clinical Trial Assistants, leading CTA study teams, and supporting clinical monitoring and process-improvement initiatives.

Location: Bangkok, Thailand

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 within project timelines.
  • Prepare, distribute, file, archive, and periodically review clinical documentation and reports according to standard operating procedures.
  • Coordinate clinical trial supplies, Case Report Forms, queries, and clinical data-flow tracking.
  • Serve as a central contact for project communications, correspondence, and associated documentation.
  • Mentor and onboard less experienced Clinical Trial Assistants, and may lead CTA study teams.
  • Support CRA site visits, clinical monitoring duties, interviewing, and quality or process-improvement initiatives after completing required training.

Requirements

  • High school diploma or equivalent, plus administrative support experience.
  • At least two years of clinical research experience is strongly preferred.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.
  • Good command of English, with effective written and verbal communication skills.
  • Strong time-management, organizational, and relationship-building skills.
  • Knowledge of Good Clinical Practice, ICH guidelines, and applicable protocol requirements.

Culture & Benefits

  • Full-time employment in a clinical research services environment.
  • Collaboration with Clinical Research Associates and Regulatory and Start-Up teams.
  • Training provided on applicable regulatory and protocol requirements.

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