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Clinical Trials Volunteer jobs in Toronto, ON

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    • Prior experience in clinical research coordination (dermatology or clinical trial experience is an asset).
    • Comfortable working with clinical staff, patients,…
    • The Clinical Research Coordinator will play a central role in the management and execution of clinical trials at FACET Dermatology.
    • Prior experience with multi-site clinical trials is an asset.
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    • May act as a lead clinical manager alongside other clinical managers for the execution of large-scale international clinical trials.
    • HOOPP Pension Plan (Defined Benefits Pension).
    • Generous vacation days for permanent and long-term contracts.
    • Support the coordination and development of CIHI’s…
    • Strong knowledge of clinical research terminology.
    • You are a team player with excellent communication, critical thinking and prioritization skills.
    • Employment Type: Full time, Permanent.
    • Responsible for the management of the Trial Master File (TMF) content and associated processes during the study life…
    • 1-3 years direct full-time experience in clinical trials TMF management.
    • Ensure proper management of essential clinical trial documentation.
    • Ensures consistency of clinical study and processes across clinical trials, overseeing and resolving operational aspects of clinical trials in conjunction with…
    • Supervising project team members in planning, conducting and evaluating clinical trials.
    • You will participate in weekly clinical and scientific meetings related…
    • Experience in administering and conducting clinical trials from startup to closeout.
    • SOCRA/CCRP or ACRP certification preferable/ completion of a clinical…
    • In this dynamic clinical operations co-op position at Oncoustics you will gain hands-on experience in coordinating and optimizing clinical trials, ensuring…
    • 2+ years of experience in clinical research coordination, clinical operations, or a related role.
    • Ensure study activities follow HIPAA and applicable clinical…
    • M.Sc. degree with adequate knowledge of conducting clinical trials.
    • Minimum B.Sc. degree with 1 year experience in conducting clinical trials or;
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Clinical Trial Coordinator- Senior (1 Yr Contract)
245 West Beaver Creek Road, Richmond Hill, ON L4B 1L1
$35–$37 an hour
Contract

Job details

$35–$37 an hour
On-site parking
Contract
245 West Beaver Creek Road, Richmond Hill, ON L4B 1L1

Full job description

About Us

We are a busy full-service dermatology practice in Richmond Hill, ON, dedicated to providing exceptional patient care alongside a growing clinical research program. We are seeking a detail-oriented and motivated Contract Senior Research Coordinator to support our clinical trials team. The contract Senior Research Coordinator role has the potential to be converted to a full-time position. This would be discussed closer to the end of the contract.

Position Overview

The Contract Research Coordinator will play a key role in coordinating and supporting dermatology clinical research studies, ensuring compliance with regulatory standards, protocol adherence, and high-quality data collection throughout the study lifecycle.

Key Responsibilities

  • Coordinate day-to-day activities of clinical research studies, including patient recruitment, screening, and scheduling
  • Assist with informed consent processes and ensure participant understanding of study requirements
  • Maintain accurate and complete source documents and case report forms (CRFs)
  • Ensure studies are conducted in accordance with Good Clinical Practice (GCP), Health Canada regulations, and sponsor protocols
  • Liaise with sponsors, monitors, and the research team to support site visits, audits, and monitoring activities
  • Manage study supplies, drug/device accountability, and regulatory documentation (essential documents, IRB/REB submissions)
  • Support data entry, query resolution, and adverse event reporting
  • Maintain organized and audit-ready regulatory binders and study files
  • Assist with pre-study, initiation, monitoring, and close-out visits

Qualifications

  • Post-secondary education in life sciences, nursing, or a related health field
  • Prior experience in clinical research coordination (dermatology or clinical trial experience is an asset)
  • Knowledge of GCP/ICH guidelines and Health Canada regulatory requirements
  • Strong organizational skills and attention to detail
  • Excellent written and verbal communication skills
  • Comfortable working with clinical staff, patients, and external sponsors/monitors
  • Proficiency with electronic data capture (EDC) systems and Microsoft Office

What We Offer

  • Hands-on experience in a growing dermatology research program
  • Collaborative, supportive team environment
  • Opportunity to build expertise in clinical trial operations
  • The contract Senior Research Coordinator role has the potential to be converted to a full-time position. This would be discussed closer to the end of the contract.

How to Apply

Please submit your resume and a brief cover letter outlining your relevant experience to manager@yorkderm.ca

York Dermatology Clinic and Research Centre is committed to fostering an inclusive and accessible workplace. Accommodations are available upon request throughout the recruitment process.

Pay: $35.00-$37.00 per hour

Expected hours: No more than 40.0 per week

Benefits:

  • On-site parking

Ability to commute/relocate:

  • Richmond Hill, ON L4B 1L1: reliably commute or plan to relocate before starting work (preferred)

Education:

  • Bachelor's Degree (required)

Language:

  • English (required)

Work Location: In person

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