Senior Research Assistant - TCM

Kwantlen Polytechnic University (KPU) is Canada's only polytechnic university, proudly serving the South Fraser region for more than 40 years. With campuses in Surrey, Richmond, Langley, and Cloverdale, KPU is deeply connected to the communities it serves and to the diverse cultures, backgrounds, and lived experiences of its students. Through academic excellence, applied learning, innovation, and strong industry and community partnerships, KPU prepares students for meaningful futures.

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We invite you to explore your next career opportunity at KPU and discover how your work can contribute to a university where thought truly meets action.

Competition :  4806  Internal Closing Date:  September 11, 2026  External Closing Date:  September 11, 2026  # of Openings:  1  
* Salary Information:  Casual Employee - Hourly Rate

Employment Type:

Temporary Part Time  Workplace Type:  Hybrid  Travel Frequency:
Employee Group:  Casual Employee  Days of Work (BCGEU):
Hours of Work (BCGEU):
Hours per Week (BCGEU):

ORGANIZATIONAL STRUCTURE
This role reports to Dr. John Yang.

SUMMARY
The Senior Research Assistant will support a double-blind placebo-controlled clinical study evaluating the effectiveness of a Traditional Chinese Medicine (TCM) intervention for urinary incontinence among older adults. The study involves participant recruitment, screening, enrollment, informed consent, clinical assessments, follow-up visits, and data collection to evaluate treatment outcomes.

The Senior Research Assistant will support study implementation by assisting with participant-related activities, conducting assessments, maintaining study documentation, ensuring confidentiality, and following approved research protocols ethical requirements, and study procedures throughout the clinical trial.

KEY RESPONSIBILITIES

Support participant recruitment and screening activities under the direction of the Principal Investigator, including identifying potential participants and assisting with eligibility assessment based on approved study inclusion and exclusion criteria.

Assist with participant screening procedures under the supervision of the Principal Investigator, including collecting relevant information related to medical history, contraindications, allergies, and other safety considerations.

Support communication with potential participants regarding the study, including providing approved information about the study purpose, procedures, potential risks, and benefits, as directed by the Principal Investigator.

Support the informed consent process with eligible participants under the direction of the Principal Investigator, including reviewing approved consent forms, explaining study procedures, answering procedural questions, documenting consent, and ensuring participants have adequate time to consider participation before enrollment.

Complete participant enrollment procedures following informed consent, including assigning unique study identification codes and maintaining study tracking records.

Provide study-related instructions to enrolled participants under the approved protocol, including explaining intervention procedures, scheduled study visits, required assessments, and completion of study questionnaires.

Conduct baseline assessments, including collection of demographic information, relevant medical history, urinary incontinence symptom measures, and quality-of-life questionnaires according to the approved study protocol.

Coordinate scheduled study visits and conduct follow-up assessments, including reviewing participant diaries and medication logs, administering follow-up questionnaires, collecting outcome data, and documenting study-related information while maintaining the integrity of the double-blind study design.

Monitor and document participant-reported adverse events, side effects, or changes in health status, and promptly report safety concerns or participant issues to the Principal Investigator for assessment and follow-up.

Conduct end-of-study assessments and support study close-out procedures, including final data collection, completion of study documentation, and providing participants with information regarding access to study findings where applicable.

Maintain accurate study records, including secure handling of consent forms, participant data, and research documentation while ensuring compliance with approved research procedures, confidentiality requirements, and data management standards.

Assist with other study-related tasks as assigned…