# 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/FSP-CRA-I-Wuhan-_266087?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_c3f164a8-1a7

## Description

We are seeking a Clinical Research Associate to join our team. 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 study staff have received proper materials and instructions to safely enter patients into the study

- Verify informed consent procedures and protocol requirements are adhered to

- Review source documents to ensure data integrity

- Monitor data for missing or implausible data

- Perform monitoring tasks efficiently according to SOPs and guidelines

- 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

- Manage registry management as prescribed in project plans

- Undertake feasibility work when requested

- Participate in Quality Control Visits

- Recruit potential investigators and prepare EC submissions

- Track and follow-up on Serious Adverse Event reporting

- Independently perform CRF review and query generation

- Assist with training 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

- 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
- clinical trial management system
- medical and clinical research terminology
- attention to detail

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