# Clinical Research Associate

**Company**: Fortrea
**Work arrangement**: hybrid
**Experience**: mid
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Seoul/CRA-I_264522?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_11dba03e-04e

## Description

We are seeking a Clinical Research Associate to take on site monitoring and site management responsibilities for clinical studies. You will ensure the implementation of project plans, monitor study sites, and liaise with vendors.

**Responsibilities:**

- Conduct routine monitoring and closeout of clinical sites

- Maintain study files and conduct pre-study and initiation visits

- Liaise with vendors and other stakeholders

- Ensure study staff have received proper materials and instructions

- Verify informed consent procedures and protocol requirements

- Review data for missing or implausible entries

- Monitor data and ensure audit readiness

- Travel may be required, including air travel

- Prepare accurate and timely trip reports

- Interact with internal work groups to evaluate needs and resources

- Act as contact for clinical trial supplies and vendors

- Manage registry management and feasibility work

- Participate in Quality Control Visits and track Serious Adverse Events

- Independently perform CRF review and query generation

- Assist with training and mentoring new employees

- Coordinate clinical projects as a Local Project Coordinator

**Qualifications:**

- University or college degree in a related allied health profession

- Basic knowledge of Regulatory Guidelines and clinical trial process

- Fluent in local office language and English

- Six months experience in a related role

- Valid Driver's License

**Preferred Qualifications:**

- Additional experience in a related field

- On-site monitoring experience

- Ability to maintain confidentiality and demonstrate attention to detail

- Understanding of medical and clinical research terminology

- Experience using a clinical trial management system

## Skills

### Required
- Regulatory Guidelines
- clinical trial process
- English
- local office language

### Nice to have
- on-site monitoring
- confidentiality
- attention to detail
- medical terminology
- clinical trial management system

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Seoul/CRA-I_264522?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)