# Clinical Research Associate

**Company**: Fortrea
**Location**: Taipei
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Taipei/Clinical-Research-Associate--Taipei-_252020?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_2a7dcba3-dfd

## Description

Fortrea is seeking a Clinical Research Associate to monitor and manage clinical study sites according to company and sponsor standard operating procedures and regulatory guidelines.

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

- 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

- Performing CRF review and query generation and resolution

- Assisting with training and development of new employees

- Coordinating designated clinical projects as a Local Project Coordinator

The ideal candidate will have:

- A B.A./B.S. degree with a strong emphasis in science and/or biology

- At least 2 years of direct site monitoring experience in a bio/pharma/CRO

- Basic knowledge of regulatory guidelines and the clinical trial process

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

- Experience using IVRS, EDC, TMF, and other systems

- Good planning, organization, and problem-solving skills

- Ability to work within a project team and efficiently in a matrix environment

## Skills

### Required
- clinical research
- regulatory guidelines
- site monitoring
- data review
- IVRS
- EDC
- TMF

---

Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Taipei/Clinical-Research-Associate--Taipei-_252020?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)