💼 Full-Time Position

Clinical Research Associate I/II/Senior - FSP

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Parexel
📍 Taiwan, Taiwan, Taiwan
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Location
Taiwan, Taiwan
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Posted
June 20, 2026
Type
Full-Time
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Full-Time Opportunity: This is a permanent, full-time position with a competitive package and real career growth potential.

Job Description

When our values align, there's no limit to what we can achieve.
 

Key Accountabilities:

Site Management Responsibilities

  • Contributes to the selection of potential investigators.

  • In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission of proper application/documents to EC/IRB and to Regulator Authorities for start-up and for the duration of the study.

  • Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.

  • Confirms that site staff have completed and documented the required training appropriately, including ICH-GCP training, prior to and for the duration of the study. Ensures the sites are inspection ready at all times.