# 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/Nanjing/FSP-CRA-I-II-S-Nanjing-Hefei-_266083?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_f29a67c2-97e

## Description

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

The successful candidate will be responsible for:

- Conducting routine monitoring and closeout of clinical sites

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

- Liaising with vendors and ensuring the implementation of project plans

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

- Reviewing 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, resources, and timelines

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

- Managing investigator site budgets

- Tracking and following up on Serious Adverse Event reporting

- Independently performing CRF review and query generation

- Assisting with training and development of new employees

- Coordinating designated clinical projects as a Local Project Coordinator

The ideal candidate will have:

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

- 1 year of experience in a clinical monitoring related role

- Basic knowledge of Regulatory Guidelines and the clinical trial process

- Fluent in local office language and in English

- Good planning, organisation, and problem-solving skills

- Valid Driver's License

Preferred qualifications include:

- 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
- local office language

### Nice to have
- medical and clinical research 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/Nanjing/FSP-CRA-I-II-S-Nanjing-Hefei-_266083?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)