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    Research Technician - VancouverUBC, Canada - University of British Columbia

    University of British Columbia
    University of British Columbia VancouverUBC, Canada

    Found in: beBee S2 CA - 2 weeks ago

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    Description


    Staff – Non Union

    Job Category
    Non Union Technicians and Research Assistants

    Job Profile
    Non Union Hourly – Research Assistant /Technician 2

    Job Title
    Research Technician

    Department
    Brubacher Laboratory Department of Emergency Medicine Faculty of Medicine

    Compensation Range
    $25.89 – $30.80 CAD Hourly

    Posting End Date
    March 29, 2024

    Note: Applications will be accepted until 11:59 PM on the day prior to the Posting End Date above.

    Job End Date

    Mar 31, 2025

    This position is expected to be filled by promotion/reassignment and is included here to inform you of its vacancy at the University.

    This position is located within a health-care facility, therefore, the successful candidate will be required to provide verification of full vaccination against Covid-19 provided prior to the start date, as required by a provincial health mandate.

    At UBC, we believe that attracting and sustaining a diverse workforce is key to the successful pursuit of excellence in research, innovation, and learning for all faculty, staff and students. Our commitment to employment equity helps achieve inclusion and fairness, brings rich diversity to UBC as a workplace, and creates the necessary conditions for a rewarding career.

    Job Description Summary

    Laboratory technicians will analyze blood samples for the National Drug Driving Study, a Transport Canada / Public Safety Canada funded study investigating the prevalence of drug use in injured drivers and passengers who are treated in hospital after a motor vehicle collision. The incumbents will follow study procedures to prepare whole blood samples for toxicology analysis. They will then analyze samples using gas chromatography flame ionization detection (GC-FID) and liquid chromatography-tandem mass spectrometry (LC-MS/MS) samples and report results.

    The incumbents will follow testing protocol and procedures developed by our laboratory consultant. Technical questions related to the laboratory analysis will be answered by the laboratory consultant. They will be directly supervised by the National Drug Driving Study Project Manager and report to project Principal Investigator (PI). The incumbents will be responsible for learning and adhering to all study procedures. They are required to protect study participants' privacy and confidentiality and behave professionally in their interactions with other team members. They will be part of a larger team of Road Safety and Public Health researchers and may be asked to participate in other ongoing studies or to perform literature reviews.

    Organizational Status

    This study is managed through the UBC Department of Emergency Medicine Research at Vancouver General Hospital (VGH). The National Drug Driving Study obtains "left over" whole blood samples from injured drivers or passengers and analyzes them for alcohol, cannabinoids and a panel of other impairing substances including CNS stimulants and CNS depressants. The study also collects routine demographic and clinical information. The study has obtained funding from CIHR, Health Canada, Transport Canada and several provincial governments. Public Safety Canada funding will support the study beginning in spring 2023. Road Safety Research is one of the key strategic initiatives of the UBC Department of Emergency Medicine.

    Work Performed

    • Follows all study procedures and safety guidelines
    • Prepares blood samples for analysis following procedures to extract cannabinoids and other drugs.
    • Analyses prepared samples using LC-MS/MS and GC-FID
    • Identify and troubleshoot problems in consultation with laboratory consultant and Project Manager
    • Enters data accurately
    • Ensuring appropriate confidentiality in alignment with UBC guidelines and study procedures
    • Assist project coordinator with communication with study sites (especially around issues related to blood collection or handling)
    • Reports on progress and troubleshoots to ensure deadlines are met
    • May also be asked to conduct literature reviews including systematic reviews
    • Assists in revision of study protocols and standard operating procedures

    Consequence of Error/Judgement

    The incumbent should be able to conduct all research activities in an ethical manner suited to the proper activities of VGH and UBC as well as to the professional organizations governing themselves and those governing the activities of the Divisional Research Director and other investigators. The Research Assistant is expected to use excellent judgement to inform the PI, Research Associate, Project Manager and laboratory consultant of any unforeseen or abnormal outcomes, which could impact the study. Data collected and recorded as part of a clinical study must be detailed and accurately reflect the work performed. Medical records and proprietary information are highly confidential and must be handled with the utmost discretion. Records are released only under strict supervision of PI. An error or incorrect decision when conducting a research project may result in a protocol violation, causing inappropriate data and skewed study results. This may have financial implications such as loss of funding. Inappropriate release of confidential information on study participants may have adverse legal implications.
    Supervision Received
    The incumbent will receive training and supervision from the Laboratory Consultant and Project Manager and will perform assigned task independently after initial training.

    Supervision Given

    The incumbent may be asked to train new co-op students or laboratory technicians.

    Minimum Qualifications
    High school graduation, some additional training in a related field and a minimum two years of related experience or an equivalent combination of education and experience.
    – Willingness to respect diverse perspectives, including perspectives in conflict with one's own

    – Demonstrates a commitment to enhancing one's own awareness, knowledge, and skills related to equity, diversity, and inclusion

    Preferred Qualifications

    • Knowledge in or experience with clinical research in a laboratory setting
    • Knowledge in Microsoft Office and other computer technical skills
    • Capacity and ability to learn new software, research methods, and work routines
    • Strong verbal and written communication skills
    • Ability to adhere to ethical guidelines for research
    • Ability to work independently without direct supervision
    • Ability to multi-task and prioritize effectively
    • Ability to exercise appropriate tact, discretion, judgment, and confidentiality
    • Demonstrated commitment to valuing diversity and contributing to an inclusive working and learning environment

    View or Apply

    To help us track our recruitment effort, please indicate in your cover/motivation letter where ) you saw this job posting.


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