# Clinical Research Associate

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

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Singapore/CRA-2_264824?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_71043ecf-fe1

## Description

## Job Summary

We are seeking a Clinical Research Associate to join our team in Singapore. As a Clinical Research Associate, you will be responsible for site management and monitoring of clinical trials.

## Responsibilities

- Manage clinical studies according to Fortrea's Standard Operating Procedures, ICH GCP Guidelines, and Sponsor requirements

- Conduct site monitoring visits, including pre-study, site initiation, process monitoring, routine monitoring, and close-out visits

- Prepare and implement project plans related to Clinical Monitoring responsibilities

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

- Safeguard data integrity by reviewing source documents, generating queries, and resolving issues

- Confirm site regulatory documents and eTMF/Sponsor documents are complete and current

- Ensure adherence to global quality control and CRA performance metrics

- Travel to study sites, which may include international travel, and prepare trip reports

- Work closely with the study team to ensure study deliverables are met

## Qualifications

- University or college degree in a related allied health profession (e.g., nursing licensure)

- Thorough understanding of ICH GCP Guidelines and local regulatory requirements

- Basic understanding of the clinical trial process

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

- At least 2 years of Clinical Monitoring experience

## Preferred Qualifications

- Thorough working knowledge of Fortrea SOPs for site monitoring

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

- Phase I monitoring experience

- Life Science or Nursing qualification

- Good computer literacy with working knowledge of PCs, Windows, and Microsoft Office applications

## Physical Demands/Work Environment

- Must be able to sit at a computer for long periods

- Must be able to use hands to finger, handle or touch objects, tools or controls

- Standard office and/or home working environment

- Clinical Research Unit and hospital environment (administrative only)

- Risk of eye strain

- Will involve outside of normal office hours as required by the role

- Travel Requirement is 60% of the time (travelling to study sites)

## Skills

### Required
- ICH GCP Guidelines
- Clinical Monitoring
- Site Management
- Data Integrity

### Nice to have
- Fortrea SOPs
- Phase I monitoring
- Life Science or Nursing qualification
- Microsoft Office applications

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Singapore/CRA-2_264824?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)