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Clinical Research Volunteer jobs in Toronto, ON

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    • Collaborate closely with dermatologists, nurses, and clinic staff to integrate research into clinical workflows.
    • Registered Practical Nurse (RPN) required.
    • 2-3 years of experience in clinical trials, research coordination, or related clinical roles (Phase 1-4 clinical trial experience is an asset).
    • A Bachelors’ degree in health science, physical or biological fields with at least 3 years’ experience in clinical trial data processing and management.
    • The Schizophrenia Division at Centre for Addiction and Mental Health (CAMH) focuses on improving the understanding, treatment, and prevention of schizophrenia…
    • View all CAMH jobs - Toronto jobs - Research Assistant jobs in Toronto, ON
    • Salary Search: Research Assistant 2 - Schizophrenia Division Research salaries in Toronto, ON
    • See popular questions & answers about CAMH
    • Knowledge of clinical trial guidelines, regulatory frameworks, and research ethics requirements.
    • Demonstrated expertise in clinical trial design and…
  • View similar jobs with this employer
    • 7+ years of clinical research experience, with proven global trial management and portfolio-level oversight with a minimum of 3 years in clinical operations…
    • A Bachelors’ degree in health science, physical or biological fields with at least 3 years’ experience in clinical trial data processing and management.
    • Knowledge of quality principles and/or research ethics guidelines preferred.
    • Maintains electronic records including databases, lists, and other mechanisms that…
    • 50% of salaried time is protected for research with 50% of salaried time for clinical practice.
    • The BRI brings together teams of top researchers and trainees…
    • Dr. Munce's program of research focuses on improving transitional care for youth with complex needs and their families, advancing the meaningful engagement of…
    • SOCRA/CCRP or ACRP certification preferable/ completion of a clinical research graduate certificate.
    • Experience in administering and conducting clinical trials…
    • Have phlebotomy training and demonstrated experience independently performing blood draws in a clinical, laboratory, or research setting.
    • Have at least 3 years of clinical research experience, including demonstrated experience coordinating studies and conducting participant visits.
    • Streamline remote data collection with clinical research partners.
    • Prior research experience in the biomedical field.
    • Support QA of company solutions.
    • 2+ years of experience in clinical research coordination, clinical operations, or a related role.
    • Ensure study activities follow HIPAA and applicable clinical…
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Clinical Research Nurse Coordinator
710 Kingston Road, Toronto, ON M4E 1R7

Job details

Here’s how the job details align with your profile.

Pay

From $70,000 a year

Job type

Full-time

Benefits

Pulled from the full job description
Paid time off
Vision care
Dental care

Full job description

About FACET Dermatology

FACET Dermatology is a leading, patient-focused dermatology clinic dedicated to delivering evidence-based, innovative care for a wide range of skin conditions. Our practice integrates clinical excellence with high-quality research, offering patients access to advanced therapies through participation in clinical trials.

We are currently seeking an experienced and motivated Clinical Research Nurse Coordinator (CRC) to join our growing research team and support the advancement of dermatologic science and patient care.

Position Summary

The Clinical Research Coordinator will play a central role in the management and execution of clinical trials at FACET Dermatology. This position oversees all aspects of dermatology research studies—from study start-up through closeout—while ensuring compliance with regulatory, ethical, and clinical standards.

Key Responsibilities

  • Coordinate day-to-day clinical trial operations, including participant recruitment, screening, enrollment, and follow-up
  • Serve as the primary liaison for study sponsors, monitors, and regulatory bodies
  • Maintain accurate study documentation, including source documents, case report forms, and regulatory binders
  • Ensure compliance with study protocols, ICH-GCP guidelines, and Health Canada/FDA regulations
  • Schedule and conduct study visits, collect and process biological samples, and monitor patient safety
  • Prepare and submit regulatory documents, ethics applications, and protocol amendments
  • Provide clear, compassionate patient education and obtain informed consent
  • Collaborate closely with dermatologists, nurses, and clinic staff to integrate research into clinical workflows
  • Support audits, monitoring visits, and site inspections
  • Maintain confidentiality and data integrity for all study participants

Qualifications

  • Minimum 2 years of clinical research coordination experience (dermatology experience is an asset)
  • Strong knowledge of clinical trial regulations, ethics, and Good Clinical Practice (GCP)
  • Excellent organizational and multitasking skills with strong attention to detail
  • Professional communication skills (verbal and written)
  • Experience with electronic data capture (EDC) systems
  • Ability to work independently in a fast-paced clinical environment
  • Registered Practical Nurse (RPN) required

Why Join FACET Dermatology?

  • Be part of a forward-thinking clinic at the intersection of patient care and research
  • Contribute to studies that shape the future of dermatologic treatment
  • Work alongside a collaborative and supportive healthcare team
  • Opportunities for professional growth and certification

Job Type: Full-time

Pay: From $70,000.00 per year

Benefits:

  • Dental care
  • Paid time off
  • Vision care

Experience:

  • research: 1 year (required)

Licence/Certification:

  • Registered Practical Nurse (required)

Location:

  • Toronto, ON M4E 1R7 (preferred)

Work Location: In person

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