# 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/Beijing/FSO-CRA-I--Beijing-Tianjin-Shijiazhuang-_265990?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_1f283051-ff6

## 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 for quality and integrity

- Perform monitoring tasks efficiently and manage travel expenses

- Prepare accurate and timely trip reports

- Interact with internal work groups and act as contact for suppliers

- 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 development of new employees

- Coordinate clinical projects and act as local client contact

**Qualifications:**

- University or college degree in a related field (e.g., nursing licensure)

- Basic knowledge of Regulatory Guidelines and clinical trial process

- Fluent in local office language and English

- Six months experience in a related role (e.g., site management, study coordinator)

- Valid Driver's License

**Preferred Qualifications:**

- Additional experience in a related field (e.g., medical, clinical, pharmaceutical)

- 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 (CTMS)

## Skills

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

### Nice to have
- medical terminology
- clinical research processes
- CTMS
- customer service

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/FSO-CRA-I--Beijing-Tianjin-Shijiazhuang-_265990?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)