• Clinical Research Associate II

    Job Location(s) HK
    Job Number
    Job Category
    Clinical Research Associates
    Position Type
  • Job Overview

    Are you an exceptional Clinical Research Associate (CRA) based in Hong Kong that has independent trial site monitoring experience and would like to experience working as a CRA at a global CRO?

     Clinical Research Associates manage all aspects of study site monitoring according to Client SOP, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files.


    -Responsible for all aspects of study site visits and site management and monitoring activities ex. f/u SAE, clinical supply, etc

    -Prepare accurate and timely trip report

    -review progress of projects and initiate appropriate actions to achieve targets

    -feasibility work, site selection, EC submission, RA submission, translation of study documents, negotiate study budget, contract


    -University degree with pharmacy or medical related background preferred

    -candidate with 2 or more relevant CRA experience in pharma or CRO

    -thorough knowledge of ICH GCP and regulatory

    -Fluent in local language and English


    - 2 or more years CR experience in pharma or CRO

    - Excellent monitoring skill, site management skill, communication skills

    - Ability to work independently

    - Good planning and organization skill, computer skills



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