5 часов назад
CTA-KunTuo
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
CTA-KunTuo (Clinical Research Administration): Maintaining accurate Trial Master File records and supporting clinical research documentation, supplies, and data-flow tracking with an accent on regulatory compliance, document completeness, and project timelines. Focus on reviewing study files, coordinating clinical communications, managing Case Report Forms and queries, and supporting Clinical Research Associates during site visits.
Location: Beijing, China
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Maintain and update clinical documents and systems, including Trial Master File records, to track site compliance and performance within project timelines.
- Prepare, distribute, file, and archive clinical documentation and reports in line with project requirements and standard operating procedures.
- Review study files for completeness and support the tracking and management of Clinical Trial Supplies.
- Track Case Report Forms, queries, and clinical data flow.
- Coordinate designated project communications, correspondence, and related documentation for the clinical team.
- Support Clinical Research Associates during site visits and clinical monitoring activities after completing required training.
Requirements
- High school diploma or equivalent.
- At least 3 years of administrative support experience, or an equivalent combination of education, training, and experience.
- Working knowledge of Microsoft Word, Excel, and PowerPoint.
- Good written and verbal English communication skills.
- Effective time-management, organizational, and relationship-building skills.
- Awareness of Good Clinical Practice and International Conference on Harmonization guidelines, plus knowledge of applicable clinical trial protocol requirements.
Culture & Benefits
- Full-time employment in a clinical research organization.
- Collaboration with Clinical Research Associates and Regulatory and Start-Up teams.
- Training provided on applicable regulatory and protocol requirements.
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