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Clinical Research Coordinator

Job in Vancouver, BC, Canada
Listing for: Socket.dev
Full Time position
Listed on 2026-08-17
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research, Research Scientist
Salary/Wage Range or Industry Benchmark: 5692 - 8179 CAD Monthly CAD 5692.00 8179.00 MONTH
Job Description & How to Apply Below

Staff
- Non Union Job Category

M&P - AAPS

Job Profile

AAPS Salaried
- Research and Facilitation, Level A

Job Title

Clinical Research Coordinator

Department

Fairbairn Laboratory | BC Centre for Substance Use | Faculty of Medicine

Compensation Range

$5,692.25 - $8,179.50 CAD Monthly

The Compensation Range is the span between the minimum and maximum base salary for a position. The midpoint of the range is approximately halfway between the minimum and the maximum and represents an employee that possesses full job knowledge, qualifications and experience for the position. In the normal course, employees will be hired, transferred or promoted between the minimum and midpoint of the salary range for a job.

Posting

End Date

September 29, 2026

Note

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

Job End Date

September 30, 2027

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 Clinical Research Coordinator coordinates and completes defined elements of professional clinical research work supporting the day to day execution of clinical research studies conducted at the British Columbia Centre on Substance Use (BCCSU). Working under the general direction of the Principal Investigator(s) and in collaboration with multidisciplinary research teams, the incumbent ensures that assigned research activities are completed in accordance with approved study protocols, institutional policies, ethical standards, Good Clinical Practice (GCP) guidelines and applicable regulatory requirements.

The Clinical Research Coordinator coordinates participant recruitment and retention activities; facilitates study visits; maintains essential study and regulatory documentation; collects, monitors and manages clinical research data; supports ethics and regulatory submissions; and manage study timelines, recruitment targets and project milestones. The incumbent also serves as a liaison among investigators, study participants, sponsors and collaborating partners. The position contributes to the effective implementation and completion of clinical research studies focused on substance use, addiction medicine and related health outcomes.

Organizational

Status

This position is located at the British Columbia Centre on Substance Use (BCCSU), a provincially networked organization with a mandate to develop, implement and evaluate evidence based approaches to substance use and addiction. As a University of British Columbia Faculty of Medicine Centre, the BCCSU's vision is to transform substance use policies and care in British Columbia by translating research into education and evidence based clinical care guidance.

Through the collaborative development of evidence based policies, guidelines and standards, the BCCSU seeks to improve the integration of best practices across the continuum of substance use care. The BCCSU carries out this mandate through three integrated functions: research and evaluation, education and training, and clinical care guidance.

The Clinical Research Coordinator reports to the Principal Investigator(s) and works closely with the Research Manager, clinicians, research staff, students and community partners. The position is primarily located at the Rapid Access Addiction Clinic l's Hospital and the BC Centre on Substance Use, with some flexibility for hybrid work.

Work Performed
  • Coordinates the day to day execution of clinical research study activities in accordance with protocols, Good Clinical Practice, institutional policies and applicable regulatory requirements.
  • Manage participant recruitment and retention activities and screens, recruits and enrolls eligible study participants.
  • Manage informed consent procedures and ensures that required consent documentation is accurately completed and maintained.
  • Schedules and conducts study visits, assessments, questionnaires and follow up…
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