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    Clinical Trial Coordinator- Regulatory - Surrey, BC, Canada - Fraser Health

    Fraser Health
    Fraser Health Surrey, BC, Canada

    1 week ago

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    Description
    The salary range for this position is CAD $33.Why Fraser Health?

    Fraser Health is responsible for the delivery of hospital and community-based health services to over 1.9 million people in 20 diverse communities from Burnaby to Fraser Canyon on the traditional territories of the Coast Salish and Nlaka'pamux Nations.

    Our team of nearly 45,000 medical staff and volunteers is dedicated to serving our patients, families and communities to deliver on our vision:

    All new hires to Fraser Health must have full COVID 19 vaccination (have received a full series of a World Health Organization "WHO" approved vaccine against infection by SARS-COV-2, or a combination of approved WHO vaccines).

    Please note this applies to all postings, and individual medical exemptions must be approved by the Provincial Health Officer.

    We are committed to planetary health, we value diversity in the work force and seek to maintain an environment of Respect, Caring and Trust.

    Like us on Facebook (@fraserhealthcareers), follow us on Twitter & Instagram (@FHCareer), or connect with us on LinkedIn (fraserhealthcareers) for first-hand employee insights.


    The Coordinator, Clinical Research coordinates, conducts, and oversees clinical trials and research activities for Fraser Health (FH). Supports and facilitates the planning, communication, and implementation of clinical trials and clinical related research projects. Responsible for the recruitment of study participantsand the data collection, management,maintenance, and documentation foreach clinical study. Coordinates and conducts clinical trials and clinical related research activities for FH.
    # Assists the Leader in the design and implementation of research protocol, with the cooperation of the study sponsor.
    # Executes all aspects of study visit such as assessing adverse effects, monitoring safety, medications, questionnaires, and sample collection. Reports any adverse events per protocol or regulatory requirements.
    # Coordinates and implements all aspects of data collection and source documentation for each study. Ensures study related administrative tasks and correspondence are completed such as the preparation and collection of study and required regulatory documents. Prepares and submits applications for ethical review to the FH Research Ethics Board (REB) and other REB's, as required, and ensures that all applicable approvals for conducting research in FH and other sites are obtained.
    # Maintains, monitors, calculates, processes, and summarizes financial data, records, and information for projects.
    # Provides direction and leadership to research related staff, including the supervision of students and volunteers, within the scope of the projects, as appropriate.
    # Assists with tracking the progress of research activities against planned timelines and milestones using the Clinical Trial Management System software.
    # Baccalaureate Degree in a health related science plus three (3) years recent related experience in clinical research or an equivalent combination of education, training, and experience.


    Professional/Technical Capabilities:
    Demonstrated project management skills.
    Demonstrated technical expertise and scientific judgement.
    Ability to manage multiple research projects.
    Proficiency in the use of a personal computer (PC) and applicable software applications.
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