# Clinical Research Coordinator

**Company**: IQVIA
**Experience**: entry
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Prague-Czech-Republic/CTA2--One-Sponsor-dedicated--Prague_R1574463?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_7ceee5f2-a40

## Description

Perform daily administrative activities to ensure a complete and accurate Trial Master File delivery.

Responsibilities:

- Trial and site administration:

+ Track and report essential documents and safety reports   + Collate and distribute study tools and documents   + Update clinical trial databases and trackers   + Manage clinical supply and non-clinical supply in collaboration with other country roles   + Coordinate labeling requirements and translation change requests

- Document management:

+ Prepare documents and correspondence   + Collate, distribute, and archive clinical documents   + Assist with eTMF reconciliation and quality control   + Update manuals and documents   + Document destruction of clinical supplies   + Prepare investigator trial file binders

- Regulatory & Site Start-Up responsibilities:

+ Provide and collect forms and lists for site evaluation and validation   + Obtain and track study insurance certificates   + Support preparation of submission packages for regulatory agencies   + Publish study results where required

- Budgeting, Agreement and Payments:

+ Collaborate with finance representatives to develop country and site budgets   + Track and report negotiations   + Maintain tracking tools and contract templates   + Calculate and execute payments   + Ensure compliance with financial procedures

Qualifications:

- Completed job training or Bachelor's Degree

- Previous experience as a Trainee, CTA, or Coordinator is an advantage

- Minimum 1-2 years in Clinical Research or relevant healthcare experience

- Computer skills in Microsoft Word, Excel, and PowerPoint

- Written and verbal communication skills in Czech and English

- Effective time management and organizational skills

- Awareness of clinical research regulatory requirements, including GCP and ICH guidelines

## Skills

### Required
- Microsoft Word
- Excel
- PowerPoint
- Czech
- English
- Good Clinical Practice (GCP)
- International Conference on Harmonization (ICH) guidelines

### Nice to have
- Previous experience as a Trainee, CTA, or Coordinator

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Prague-Czech-Republic/CTA2--One-Sponsor-dedicated--Prague_R1574463?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)