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Posted 5 days ago

Clinical Research Assistant

@ UBC The University of British Columbia

Vancouver, British Columbia

Part-time3+ years experience
Apply now
SIGNALS

Overview

UBC The University of British Columbia is hiring a part-time (0.60 FTE) Clinical Research Assistant for the McKeown Lab at the Pacific Parkinson's Research Centre. The role conducts in-person study visits, reviews study data clinically, and escalates participant safety concerns to the principal investigator. The position is fixed term through November 15, 2027, on-site in Vancouver, paying $4,845.17 to $5,713.66 CAD monthly full-time equivalent.

Responsibilities:

  • Conduct in-person study visits and administer clinical assessments
  • Review study data and technology outputs from a clinical perspective
  • Identify and escalate participant safety concerns to the PI
  • Assist with participant screening, eligibility and informed consent
  • Document study activities, adverse events and protocol deviations

Requirements summary:

  • Relevant technical program or university degree, plus three years related experience
  • Clinical training in health professions preferred
  • Experience with adult patients; neurology or geriatrics an asset
  • Completion of TCPS 2 CORE and GCP training, or willingness to complete
  • Ability to work on-site in Vancouver

Tools & skills

Source and dates

Employer career site / ATS feed · workday

Employer posting date
2026-11-01
First seen by our source
2026-11-02
Source record updated
2026-11-02

These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.

Job details

SeniorityMid level
DepartmentAllied health
Experience3+ years
Travelair: none · ground: none
Work settingClient sites, Office
PositionSitting and standing
Physical demandsphysical low · computer moderate
LanguagesEnglish
Licences & certificationsTCPS 2 CORE, Good Clinical Practice
EducationBachelor’s degree (required)
Fields of studyMedicine, Nursing, Health professions

Summary and details written by AI from the posting; the employer’s posting is the authority.

UBC The University of British Columbia

FieldValue
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Job description

Job Title

Clinical Research Assistant

Job Category

Non Union Technicians and Research Assistants

Job Profile

Non Union Salaried - Research Assistant /Technician 3

Job Family Group

Staff - Non Union

Department

McKeown Laboratory Pacific Parkinson's Research Centre Division of Neurology | Department of Medicine | Faculty of Medicine

Compensation Range

$4,845.17 - $5,713.66 CAD Monthly

Job End Date

November 15, 2027

Posting End Date

November 9, 2026

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

The expected pay for this part-time, 0.60 FTE position is $2,907.10/mon, fixed term, and on-site.

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 Summary
The McKeown Lab at the Pacific Parkinson Research Centre, University of British Columbia (UBC) is seeking a part-time 0.60 FTE, Clinical Research Assistant (Digital Health) with clinical training to support a research study evaluating a digital health technology for people with Parkinson’s disease. Medical licensure in BC is not required for the position. In this role, you will contribute clinical expertise to the conduct of the study, including participant assessments, review of study data, and the identification and escalation of participant safety concerns. The position requires sound clinical knowledge, careful judgment, and the ability to work effectively with patients, caregivers, and multidisciplinary research teams.

Organizational Status
This position reports directly to the Principal Investigator (PI) and works closely with research coordinators, graduate students, postdoctoral fellows, engineers, and clinical collaborators. The Clinical Research Assistant is expected to maintain professional and respectful interactions with all team members and research participants. Given the importance of timely review of study data and participant safety, responsiveness and reliability are essential. Sensitivity and professionalism when discussing personal health matters with patient populations are critical.

Work Performed

  • 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.

Consequence of Error/Judgement
Errors in study assessments or data review may compromise the validity of the study’s findings, leading to unusable data and delays in research timelines. Poor judgment may affect participant safety, study integrity, and the reputation of the PI, the Pacific Parkinson Research Centre, and UBC.

Supervision Received
This position reports to the PI, who holds medical responsibility for the study and makes all final medical decisions, with day-to-day support from the lab manager and research coordinators. The incumbent is expected to exercise independent judgment in report review, study visits and work planning, and to escalate any clinical or safety concern to the PI.

Supervision Given
May provide guidance to trainees, students, or research staff on clinical aspects of the study, administration of study scales, and report review standards.

Minimum Qualifications
Completion of a relevant technical program or a university degree in a relevant discipline and a minimum three 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

  • 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.

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