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IQVIA · Multiple locations

# Clinical Study Administrator

Multiple locations Healthcare & Clinical 

Listed on IQVIA’s official careers site. Listed as of October 17, 2026. Check that it is still open and apply there.
[Apply on IQVIA’s careers site →](https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Hanoi-H-Ni-Vietnam/Clinical-Study-Administrator_R1568503)

[OpenNash Jobs](https://jobs.opennash.com/) / [IQVIA](https://jobs.opennash.com/companies/iqvia/) / Clinical Study Administrator

## Job description

### Job Overview

Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.

### Essential Functions

Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.

Assist with periodic review of study files for completeness. Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow. Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.

### Qualifications

High School Diploma or equivalent. 3 years administrative support experience. Equivalent combination of education, training and 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at [https://jobs.iqvia.com](https://jobs.iqvia.com) IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete.

Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

## At a glance
- Posted by the employer: Not stated
- First seen by OpenNash: Oct 10, 2026
- Last checked: Oct 17, 2026
- Listed for: 7 days
- Location: Multiple locations[Apply on IQVIA’s careers site →](https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Hanoi-H-Ni-Vietnam/Clinical-Study-Administrator_R1568503)

## More jobs at IQVIA

### [(Senior) Clinical Research Associate (CRA)](https://jobs.opennash.com/companies/iqvia/jobs/18369455a0bcaec6dd79/)

### [(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye](https://jobs.opennash.com/companies/iqvia/jobs/0e5a17bac181bde47316/)

### [Associate Director, Client Services - IQVIA Medical Communications](https://jobs.opennash.com/companies/iqvia/jobs/741a75e5f7714284464f/)

### [Associate Solution and Delivery Lead, Healthcare & Pharma](https://jobs.opennash.com/companies/iqvia/jobs/72442d5379da5a50017f/)

### [Associé(e) de recherche clinique (ARC) principal(e) / Senior Clinical Research Associate, Sponsor Dedicated](https://jobs.opennash.com/companies/iqvia/jobs/82bb761af95fb7f1ffb4/)

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Dates come from the employer where stated; “first seen” and “last checked” are our own observations.

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