# Clinical Trial Assistant

**Company**: IQVIA
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Bangkok-Thailand/Senior-Clinical-Trial-Assistant_R1571165?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_8f1dc3fe-811

## Description

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

**Essential Functions**

- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with updating and maintaining clinical documents and systems.

- Collaborate with the clinical team on preparing, handling, distributing, filing, and archiving clinical documentation and reports.

- Assist with periodic review of study files and completeness.

- Collaborate with CRAs and RSU on preparing, handling, and distributing Clinical Trial Supplies and maintaining tracking information.

- Coordinate 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.

- Mentor less experienced Clinical Trial Assistants (CTAs).

- Assist with training and onboarding new CTAs.

- May serve as a subject matter expert for business processes.

- May lead CTA study teams.

- May assist with interviewing and screening potential new team members.

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

- May participate in departmental quality or process improvement initiatives.

**Qualifications**

- High School Diploma or equivalent.

- 5 years of administrative support experience.

- Equivalent combination of education, training, and experience.

- Minimum two years of clinical research experience strongly preferred.

- Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint.

- Effective written and verbal communication skills, including good command of English.

- Effective time management and organisational skills.

- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

- Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines as provided in company training.

- Knowledge of applicable protocol requirements as provided in company training.

## Skills

### Required
- Microsoft Word
- Excel
- PowerPoint
- Good Clinical Practice (GCP)
- International Conference on Harmonisation (ICH)

### Nice to have
- clinical research
- regulatory requirements

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Bangkok-Thailand/Senior-Clinical-Trial-Assistant_R1571165?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)