# Clinical Research Associate

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

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/FSP-CRA-II--Beijing-_266102?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_3278d1d9-5dd

## Description

We are seeking a Clinical Research Associate to manage clinical studies according to Fortrea's Standard Operating Procedures, ICH GCP Guidelines, and Sponsor requirements.

The successful candidate will be responsible for:

- Conducting site monitoring responsibilities for clinical trials, including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits

- Preparing and implementing project plans related to Clinical Monitoring responsibilities

- Ensuring the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to

- Safeguarding data integrity through source document review, source document verification, query generation, and resolution

- Confirming Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current

- Guaranteeing accurate Investigational Product inventory and accountability

- Ensuring adherence to global quality control and CRA performance metrics

- Ensuring audit readiness at site level

- Acting as a Lead CRA as assigned

The ideal candidate will have:

- A university or college degree, or certification in a related allied health profession

- Thorough understanding of ICH GCP Guidelines and local regulatory requirements

- Thorough knowledge of monitoring procedures

- Basic understanding of the clinical trial process

- Fluent in local office language and in English, both written and verbal

Preferred qualifications include:

- Thorough working knowledge of Fortrea SOPs for site monitoring

- Additional years of experience in a related field

- Phase I monitoring experience

- Life Science or Nursing qualification

In return, you will receive:

- Competitive salary

- Opportunity to work on a variety of clinical trials

- Collaborative and dynamic work environment

This role requires 60% travel to study sites.

## Skills

### Required
- ICH GCP Guidelines
- clinical trial management
- source document review

### Nice to have
- Fortrea SOPs
- Phase I monitoring experience
- Life Science or Nursing qualification

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/FSP-CRA-II--Beijing-_266102?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)