Centricity Research is one of the largest clinical research networks in North America. We area fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.

About the role

We are seeking an experienced, full-time, permanent Clinical Research Coordinator (CRC) to join our ON-VAU/Vaughan site. In this role, you will independently coordinate clinical studies, conduct participant visits and phlebotomy, and work closely with Investigators and the broader research team to ensure study activities are safe, organized, accurate, and compliant with protocol and regulatory requirements.

This position is primarily based at Centricity Research Vaughan Endocrinology site in Vaughan and will also provide support to Centricity Research Toronto LMC Multispecialty and Centricity Research CPU-Toronto sites as operational needs require.

Compensation

Base salary range: $55,000-$62,500. This role is eligible for incentive compensation.

What you'll do

Study Coordination & Participant Safety

Conduct study visits in accordance with protocol, GCP, SOPs, and regulatory requirements

Ensure participant safety and well-being, reporting and documenting adverse events per protocol and regulations

Perform clinical procedures such as vitals, ECGs, sample collection/processing, and investigational product handling

Recruitment, Screening & Enrollment

Support recruitment strategies to identify and enroll eligible participants

Conduct participant screening according to protocol inclusion/exclusion criteria

Guide participants through the informed consent process and ensure proper documentation

Schedule and coordinate study visits throughout the participant lifecycle

Study Execution & Data Integrity

Accurately complete study documentation,



regulatory records, and periodic reports

Prepare for and support monitoring visits, audits, and inspections

Perform regular quality control (QC) checks on study data and source documents

Collaborate with investigators, management, and sponsors to ensure study compliance and accuracy

Contribute to site start-up activities, including feasibility questionnaires (FQs) and pre-study visits (PSVs)

Quality, Compliance & Site Support

Support lab supply inventory, equipment maintenance, and administrative needs

Assist with community engagement and outreach events as needed

You Might Be a Great Fit If You:

Have a bachelor's degree in a health, science, or research-related field, or an equivalent combination of relevant education and experience.

Have at least 3 years of clinical research experience, including demonstrated experience coordinating studies and conducting participant visits.

Have at least 3 years of hands-on phlebotomy experience and are currently qualified to perform phlebotomy in Canada.

Have robust knowledge of medical terminology, GCP, study protocols, SOPs, and clinical research documentation requirements.

Experience across multiple therapeutic areas, such as vaccines, obesity, rare diseases, or Alzheimer's disease, is considered an asset.

Are organized, detail-oriented, and skilled at prioritizing multiple responsibilities in a fast-paced environment.

Are a self-starter who can work independently, take ownership of assigned studies, and become productive quickly with limited supervision.

Are willing and able to work primarily at Centricity Research Vaughan Endocrinology site in Vaughan and provide support to Centricity Research Toronto LMC Multispecialty and Centricity Research CPU-Toronto sites as operational needs require.

The pay range for this role is:

55,000 - 62,500 CAD per year (Centricity Research Vaughan Endocrinology)

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📌 Clinical Research Coordinator (Vaughan)
🏢 Centricity Research
📍 Vaughan