Clinical Research Assistant
Research AssociateLaboratory & Life Sciences
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Quick Summary
Technical Tools
Research AssociateLaboratory & Life Sciences
Clinical Research Assistant
Non Union Technicians and Research Assistants
What We Offer
~1 min read✓Conduct in-person study visits with research participants, including administering standardized clinical assessments and questionnaires.
✓Review study data and technology-generated outputs from a clinical perspective, using structured review procedures.
✓Identify potential participant safety concerns and escalate them promptly to the PI according to study procedures.
✓Assist with participant screening, eligibility review and the informed consent process.
✓Support participants and caregivers in the use of study technologies.
✓Document study activities, adverse events and protocol deviations accurately and in a timely manner.
✓Assist with the finalization of the study protocol and regulatory materials, including Research Ethics Board (REB) submissions, consent forms, and study documentation.
✓Implement and follow standard operating procedures (SOPs), the approved study protocol, and Research Ethics Board (REB) requirements.
✓Provide clinical input to the research and development team to support the design and refinement of study tools.
✓Collaborate with multidisciplinary teams, including engineers, clinicians, and researchers, to support the study protocol, data analysis and publications.
Responsibilities
~1 min read- →A degree in medicine, nursing, or other health professions, or equivalent; international credentials considered. Medical licensure in British Columbia is not required for this role.
- →Clinical experience with adult patients; experience in neurology, movement disorders, geriatrics or psychiatry is an asset.
- →Familiarity with Parkinson’s disease and its non-motor symptoms (e.g., depression and anxiety, orthostatic hypotension, constipation).
- →Experience with clinical research, including participant recruitment, informed consent and data collection.
- →Completion of TCPS 2 CORE and Good Clinical Practice (GCP) training, or willingness to complete them before starting.
- →Comfort working with digital health tools and interest in AI in clinical care.
- →Strong attention to detail and ability to maintain high data quality standards.
- →Excellent communication and interpersonal skills are essential, including the ability to discuss sensitive health topics with older adults and their caregivers.
- →Ability to work on-site in Vancouver and to schedule study visits around participants’ availability.
Note: This position involves working with participant health information, and strict adherence to privacy and ethical guidelines is required.
If you are a medically trained professional interested in contributing to cutting-edge Parkinson’s disease research and the responsible use of AI in patient care, we encourage you to apply. Join our team in advancing innovative digital health research at UBC.
Location & Eligibility
Where is the job
Bc, Canada
On-site at the office
Who can apply
CA
About this job
- Pay per year
- ≈ CA$58,142–CA$68,564 a year
- Who can apply
- Canada
- Posted
- 6 days ago
Listing Details
- Posted
- November 3, 2026
- First seen
- November 3, 2026
- Last seen
- November 9, 2026
Posting Health
- Days active
- 5
- Repost count
- 0
- Trust Level
- 40%
- Scored at
- November 9, 2026
Signal breakdown
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