# Clinical Research Associate

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

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/FSP-CRA-I--Taiyuan-_264569?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_00eaddca-a78

## Description

We are seeking a Clinical Research Associate to oversee site monitoring and management for clinical studies. As a Clinical Research Associate, you will be responsible for ensuring the implementation of project plans, monitoring study sites, and maintaining study files.

**Responsibilities:**

- Conduct routine monitoring and closeout of clinical sites

- Maintain study files and ensure proper documentation

- 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 accuracy and completeness

- Monitor data for missing or implausible entries

- Ensure audit readiness at the site level

- Travel to clinical sites as required

- 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

- Assist with training and development of new employees

- Coordinate clinical projects as a Local Project Coordinator

**Requirements:**

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

- Basic knowledge of regulatory guidelines and clinical trial processes

- Fluent in local office language and English

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

- Valid driver's license

- Good planning, organization, and problem-solving skills

- Good computer skills with working knowledge of Microsoft Office applications

**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 processes
- site management
- study coordination
- data analysis

### Nice to have
- on-site monitoring
- confidentiality
- attention to detail
- medical terminology
- CTMS experience

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/FSP-CRA-I--Taiyuan-_264569?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)