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site activation manager, clinical research.

job details

summary

    job details

    about the company.

    Our cleint is currently seeking a full-time, office-based study Site Activation Manager to join their Clinical
    Research business in Hong Kong.

    about the team.

    To lead a team of Submission Coordinators, Principal Submission Coordinators in the Hong Kong office.

    about the job.

    • Efficiently manage and successfully execute all aspects of global start-up;
    • Perform quality checks on submission documents and site essential documents;
    • Prepare and approve informed consent forms;
    • Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
    • Present during bid defenses, general capabilities meetings, and audits.
    skills & experiences required.
    • Bachelor's degree in the science field or equivalent combination of education and experience;
    • At least five years of relevant working experience at a CRO, Pharmaceutical Company, or an investigative
    • site;
    • Excellent organization and communication skills;
    • Knowledge of Microsoft® Office, ICH - GCP guidelines and regulatory guidelines;
    • Hands-on experience preparing, reviewing, and submitting regulatory documentation to Ethics Committees
    • and Regulatory Agencies; including formulating responses to queries; and
    • Good command in English and Fluent in Cantonese.

    Interested individuals can click apply now and send through an updated resume in WORD format. For a more comprehensive list of current opportunities, please visit https://www.randstad.com/jobs/q-hong-kong/ or contact Boris Lee at + 852 2232 3497 or email boris.lee@randstad.com.hk

    about the company.

    Our cleint is currently seeking a full-time, office-based study Site Activation Manager to join their Clinical
    Research business in Hong Kong.

    about the team.

    To lead a team of Submission Coordinators, Principal Submission Coordinators in the Hong Kong office.

    about the job.

    • Efficiently manage and successfully execute all aspects of global start-up;
    • Perform quality checks on submission documents and site essential documents;
    • Prepare and approve informed consent forms;
    • Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
    • Present during bid defenses, general capabilities meetings, and audits.
    skills & experiences required.
    • Bachelor's degree in the science field or equivalent combination of education and experience;
    • At least five years of relevant working experience at a CRO, Pharmaceutical Company, or an investigative
    • site;
    • Excellent organization and communication skills;
    • Knowledge of Microsoft® Office, ICH - GCP guidelines and regulatory guidelines;
    • Hands-on experience preparing, reviewing, and submitting regulatory documentation to Ethics Committees
    • and Regulatory Agencies; including formulating responses to queries; and
    • Good command in English and Fluent in Cantonese.

    Interested individuals can click apply now and send through an updated resume in WORD format. For a more comprehensive list of current opportunities, please visit https://www.randstad.com/jobs/q-hong-kong/ or contact Boris Lee at + 852 2232 3497 or email boris.lee@randstad.com.hk