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responsible to the Clinical Research Manager. Work Performed o Responsible for subject communication, responding to phone calls and emails. o Provides direction to ensure subject visits are scheduled according
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are scheduled according to study protocol and missed visits are reported to the Coordinator and recorded in the source documents. o Coordinates recruitment of research subjects. o Coordinates scheduling
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recruitment, consent, and retention activities, such as pre-screening, scheduling, obtaining informed consent, and maintaining follow-up communication with participants, with complex cases escalated
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maintenance and safety checks as well as repairing or replacing lab and research study equipment as needed. Supervising, scheduling and training staff and student helpers and volunteers Writing reports and
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authored papers Experience with project management (creating project charters, schedules, project management plans) is considered an asset. Applications, including CV, names of two references, cover letter
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will be primarily responsible for participant recruitment, schedules, data collection, database creation, data management, and data checking under the supervision of Dr. Teresa Liu-Ambrose and will work
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maintain organized and confidential research files, records, and project materials. • Prepare recruitment materials and assist with participant communication (e.g., emails, reminders, scheduling
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assist with participant communication (e.g., emails, reminders, scheduling), including supporting participant retention strategies. • Assist with survey data collection, entry, cleaning, and basic
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supervision in carrying out duties and responsibilities, as listed, but is expected to schedule and prioritize their own work; receives instructions during orientation and will be oriented to any new activities
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and safety procedures in conjunction with data collection (including enrolling study participants, scheduling and conducting interviews with study participants as per UBC ethics protocol). Oversee data