18 дней назад
Clinical Trial Assistant
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Trial Assistant (Clinical Research): Supporting clinical teams with accurate Trial Master File maintenance, clinical documentation, trial supplies, Case Report Forms, and study data tracking with an accent on regulatory compliance, document completeness, and project timelines. Focus on coordinating clinical communications, reviewing study files, managing documentation workflows, and assisting with site monitoring activities after required training.
Location: Pasig, Philippines; onsite
Company
IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Support Clinical Research Associates and Regulatory and Start-Up teams with maintaining clinical documents and systems, including the Trial Master File.
- Prepare, handle, distribute, file, and archive clinical documentation and reports according to project scope and standard operating procedures.
- Review study files for completeness and track site compliance and performance within project timelines.
- Coordinate clinical trial supplies, Case Report Forms, queries, and clinical data flow.
- Serve as a central contact for designated project communications, correspondence, and related documentation.
- Accompany CRAs on site visits and assist with monitoring duties after completing required training.
Requirements
- High school diploma or equivalent, or an equivalent combination of education, training, and experience.
- 3–4 years of administrative support experience.
- Working knowledge of Microsoft Word, Excel, and PowerPoint.
- Good written and verbal English communication skills.
- Effective time management, organizational, and relationship-building skills.
- Basic knowledge of Good Clinical Practice, International Conference on Harmonization guidelines, and applicable protocol requirements.
Nice to have
- At least one year of clinical research experience.
Culture & Benefits
- Full-time employment.
- Work in clinical research supporting the development and commercialization of medical treatments.
- Collaboration with clinical, regulatory, and start-up teams.
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