IQVIA

CTA(Dalian)

Dalian, Liaoning, China FULL TIME Remote Friendly
The Brief

“CTA(Dalian) at IQVIA. Skills: Trial Master File, Clinical documentation, Administrative support. Perform daily administrative activities. Assist with updating and maintaining clinical documents”

What You'll Achieve.

Ensure a complete and accurate Trial Master File delivery; Track site compliance and performance within project timelines

What They're Looking For.

Must Have

Bachelor degree, 1-year administrative support experience, Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint, Written and verbal communication skills including good command of English language, Effective time management and organizational skills, Ability to establish and maintain effective working relationships with coworkers, managers, and clients, Awareness of applicable clinical research regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training, Knowledge of applicable protocol requirements as provided in company training

What You'll Do.

Perform daily administrative activities

Assist with updating and maintaining clinical documents

Assist with preparation

Assist with periodic review of study files

Assist with preparation

handling and distribution of Clinical Trial Supplies

Assist with tracking and management of Case Report Forms

Act as a central contact for project communications

Accompany CRAs on site visits

How You'll Work.

Team & Collaboration

Work with Clinical Research Associates; Work with Regulatory and Start-Up teams; Establish and maintain effective working relationships with coworkers, managers, and clients

Communication Scope

Written communication skills; Verbal communication skills; Good command of English language

Free ATS check

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