CTA (Clinical Trials)

Location: Chengdu, Sichuan, China

Company

IQVIA 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, and archive clinical documentation and reports according to project scope and standard operating procedures.
• Review study files for completeness and manage tracking information for Clinical Trial Supplies.
• Track Case Report Forms, queries, and clinical data flow.
• Serve as a central contact for designated project communications, correspondence, and related documentation.
• Accompany Clinical Research Associates on site visits and assist with clinical monitoring after completing required training.

Requirements

• Bachelor’s degree or higher, or an equivalent combination of education, training, and experience.
• 1–3 years of administrative support experience.
• Working knowledge of Microsoft Word, Excel, and PowerPoint.
• Good command of English, with strong written and verbal communication skills.
• Effective time-management and organizational skills, with the ability to maintain relationships with coworkers, managers, and clients.
• Awareness of Good Clinical Practice and International Conference on Harmonization guidelines, as well as applicable clinical trial protocol requirements.

Culture & Benefits

• Full-time employment.
• Work supporting clinical research and the development of medical treatments.
• Training is provided for applicable clinical research regulatory requirements and protocol procedures.