# Clinical Research Associate

**Company**: Fortrea
**Location**: Chengdu
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Chengdu/FSP-CRA-I-II-Chengdu-Chongqing-Guiyang--_265061?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_fd8f6a35-45e

## Description

We are seeking a Clinical Research Associate to join our team in Chengdu. As a Clinical Research Associate, you will be responsible for site monitoring and site management for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines.

**Responsibilities:**

- Conduct routine monitoring and closeout of clinical sites

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

- Liaise with vendors and perform other duties as assigned

- Ensure the protection of study patients by verifying informed consent procedures and protocol requirements

- Monitor data for missing or implausible data

- Ensure audit readiness at the site level

- Travel may be required, including air travel

- Prepare accurate and timely trip reports

- Interact with internal work groups to evaluate needs, resources, and timelines

- Act as contact for clinical trial supplies and other suppliers

- Perform registry management and feasibility work as prescribed in project plans

- Participate in Quality Control Visits and follow-up on Serious Adverse Event reporting

- Independently perform CRF review and query generation and resolution

- Assist with training, mentoring, and development of new employees

- Coordinate designated 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 in English, both written and verbal

- 1 year experience in a clinical monitoring related role

- Valid Driver's License

**Preferred Qualifications:**

- Additional experience in a related field

- On-site monitoring experience

- Ability to maintain confidentiality of data and information

- Demonstrated ability to conduct clinical operations activities effectively and efficiently

- Understanding of medical and clinical research terminology and clinical research processes

## Skills

### Required
- Regulatory Guidelines
- clinical trial process
- English

### Nice to have
- medical and clinical research terminology
- clinical research processes
- CTMS

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Chengdu/FSP-CRA-I-II-Chengdu-Chongqing-Guiyang--_265061?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)