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Coordinator, Clinical Research

Job in New Westminster, Burnaby, BC, K3L, Canada
Listing for: Fraser Health Authority
Full Time position
Listed on 2026-02-02
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
  • Research/Development
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 34.67 - 49.83 CAD Hourly CAD 34.67 49.83 HOUR
Job Description & How to Apply Below
Location: New Westminster

Salary

The salary range for this position is CAD $34.67 - $49.83 / hour

Job Summary

Join Fraser Health’s Research team and help advance innovative, evidence-based healthcare. As a Casual
Coordinator, Clinical Research in New Westminster, B.C., you will oversee and conduct clinical trials and related research activities, ensuring compliance with study protocols, ethics, and regulatory requirements.

This casual/auxiliary role works two days per week. Patients in inpatient rehab are typically seen by therapists Monday to Friday from 9 a.m. to 3 p.m., so afternoon availability is important. The successful candidate must be available on Tuesdays as one of their scheduled days.

You’ll collaborate with investigators, sponsors, and interdisciplinary teams to design and implement studies, recruit participants, manage data, and maintain accurate documentation. Your strong coordination and communication skills will support public awareness, foster collaboration, and promote research excellence.

Ideal candidates bring experience in clinical trial coordination, knowledge of research ethics and regulations, and the ability to manage multiple projects efficiently. Be part of a team driving research that improves patient outcomes and strengthens health care across Fraser Health.

A career with Fraser Health will offer you the opportunity to be a part of a dedicated team of professionals in a dynamic and rewarding health care environment. We offer a competitive compensation and benefit package, including comprehensive health benefits coverage.

Important to know

Before we can finalize any offer of employment, you must:

  • Confirm you are legally entitled to work in Canada

Take the next step and apply so we can continue the conversation with you.

Detailed Overview

Supporting the Vision, Values, Purpose and Commitments of Fraser Health including service delivery that is centered around patients/clients/residents and families:

The Coordinator, Clinical Research coordinates, conducts, and oversees clinical trials and research activities for Fraser Health (FH). Supports and facilitates the planning, communication, and implementation of clinical trials and clinical related research projects. Responsible for the recruitment of study participants and the data collection, management, maintenance, and documentation for each clinical study. Supervises and monitors study subject progress and follow-up. Ensures compliance and timelines are maintained.

This position requires travel to various sites across Fraser Health to support research activities and collaborate with site teams.

Responsibilities
  • Coordinates and conducts clinical trials and clinical related research activities for FH.
  • Provides assistance to the Leader in the development and design of evaluation processes and procedures and research protocols.
  • Provides assistance in the formulation of communication plan and public awareness strategies to proactively communicate and ensure greater public awareness and support for research activities across FH.
  • Assists the Leader in the design and implementation of research protocol, with the cooperation of the study sponsor.
  • Recruits study participants by identifying and screening potential subjects and obtaining informed consent.
  • Coordinates patient visit schedules as per study protocol. Executes all aspects of study visit such as assessing adverse effects, monitoring safety, medications, questionnaires, and sample collection. Reports any adverse events per protocol or regulatory requirements.
  • Coordinates and implements all aspects of data collection and source documentation for each study. Ensures study related administrative tasks and correspondence are completed such as the preparation and collection of study and required regulatory documents. Prepares and submits applications for ethical review to the FH Research Ethics Board (REB) and other REB's, as required, and ensures that all applicable approvals for conducting research in FH and other sites are obtained.
  • Supervises and monitors study subject progress and follow-up. Ensures compliance is maintained.
  • Maintains, monitors, calculates, processes, and summarizes financial data, records, and…
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