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CRA I - CRA II

FortreaSingaporePosted 21 May 2026

Fortrea is hiring a Clinical Research Associate in Singapore to manage clinical study site monitoring. The role involves routine monitoring, closeout of clinical sites, study file maintenance, and site management according to project plans. Candidates must have at least one year of clinical monitoring experience and a strong understanding of ICH GCP guidelines. The position requires 60% travel to study sites.

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Experience

1+ years

Function

Healthcare Services

Work mode

Onsite, Singapore

Company

Tier 2

What you will work on

Fortrea is hiring a Clinical Research Associate in Singapore to manage clinical study site monitoring. The role involves routine monitoring, closeout of clinical sites, study file maintenance, and site management according to project plans. Candidates must have at least one year of clinical monitoring experience and a strong understanding of ICH GCP guidelines. The position requires 60% travel to study sites.

TAL's take

Quality 55/1005/5 clarityTier 2 company

Established clinical research organization offering a clear role with defined monitoring responsibilities and travel requirements.

The JD provides a very clear definition of site monitoring responsibilities and qualifications required for the CRA role.

Must haves

  • University degree or allied health certification
  • Minimum 1 year clinical monitoring experience
  • Understanding of ICH GCP Guidelines
  • Knowledge of monitoring procedures
  • Ability to work with minimal supervision

Tools and skills

ich gcp guidelinesclinical monitoringsite managementsae reporting

About the company

Fortrea is a established global clinical research organization providing services to the pharmaceutical and biotech industries.

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