# Clinical Research Coordinator

**Company**: IQVIA
**Location**: Columbus, Ohio
**Job type**: full-time
**Salary**: $35,800.00 - $123,000.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Columbus-Ohio-United-States-of-America/Clinical-Trial-Assistant--HYBRID-in-Columbus--OH_R1577995?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/clinical-research-coordinator-7280e742-2b9/

## Description

We are seeking a Clinical Research Coordinator to support our clinical research team in Columbus, Ohio.

The successful candidate will assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams with maintaining clinical documents and systems, preparing and handling clinical documentation and reports, and tracking clinical trial supplies.

Key responsibilities include:

- Assisting CRAs and RSU teams with updating and maintaining clinical documents and systems

- Preparing, handling, distributing, filing, and archiving clinical documentation and reports

- Reviewing study files for completeness

- Assisting with tracking and management of Case Report Forms (CRFs), queries, and clinical data flow

- Acting as a central contact for the clinical team for designated project communications and correspondence

- Accompanying CRAs on site visits to assist with clinical monitoring duties upon completion of required training

Requirements:

- Bachelor's degree

- 3 years of administrative support experience

- Computer skills including Microsoft Word, Excel, and PowerPoint

- Good command of English language

- Effective time management and organisational skills

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

- Awareness of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

We offer a competitive salary ranging from $35,800 to $123,000 per year, depending on experience and qualifications.

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## Skills

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

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Columbus-Ohio-United-States-of-America/Clinical-Trial-Assistant--HYBRID-in-Columbus--OH_R1577995?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)