# 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--Beijing-_266100?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_e2e529f2-809

## Description

We are seeking a Clinical Research Associate to manage and monitor clinical studies at various sites.

The successful candidate will be responsible for ensuring that studies are conducted according to Company and Sponsor Standard Operating Procedures, as well as Regulatory Guidelines.

Key responsibilities include:

- Conducting routine monitoring and closeout of clinical sites

- Maintaining study files and conducting pre-study and initiation visits

- Liaising with vendors and other stakeholders

- Ensuring the protection of study patients and the integrity of data submitted

- Monitoring data for missing or implausible entries

- Ensuring audit readiness at the site level

- Preparing accurate and timely trip reports

- Interacting with internal work groups to evaluate needs and resources

- Acting as a contact for clinical trial supplies and other suppliers

- Managing investigator site budgets and tracking Serious Adverse Event reporting

- Performing CRF reviews and query generation

- Assisting with training and development of new employees

- Coordinating designated clinical projects

The ideal candidate will have:

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

- Basic knowledge of Regulatory Guidelines and the clinical trial process

- Fluent in local office language and English

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

- Good planning, organisation, and problem-solving skills

- Valid Driver's License

Preferred qualifications include:

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

- On-site monitoring experience

- Understanding of medical and clinical research terminology

- Experience using a clinical trial management system (CTMS)

## Skills

### Required
- Regulatory Guidelines
- clinical trial process
- site management
- study coordination
- data analysis

### 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/FSP-CRA-I--Beijing-_266100?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)