About the Role We are seeking a full-time Clinical Research Coordinator I (CRC I) to join our research team at ON-CPU location in Toronto. In this role, you will support the successful execution of clinical studies by performing a mix of administrative and clinical responsibilities. You will work closely with Investigators and the broader research team to ensure study activities are organized, compliant, and aligned with protocol requirements. Strong medical knowledge, clinical understanding, and phlebotomy experience are required. An international medical graduate (IMG) or internationally trained physician is preferred.

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, phlebotomy, sample collection/processing, and investigational product handling

Conduct participant screening according to protocol inclusion/exclusion criteria

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

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

Quality, Compliance & Site Support

Prepare for monitoring visits, audits, and maintain regulatory files

Perform regular quality control checks on source data and documents

Support lab supply inventory, equipment maintenance, and administrative needs

Assist with community engagement and outreach events as needed





Have a bachelor’s degree in a health, science, or research-related field (or equivalent combination of education and experience)

Are an international medical graduate (IMG) or internationally trained physician (preferred)

Have 2–4 years of experience in a healthcare setting and are comfortable with clinical tools like blood pressure monitors, ECG machines, and weight scales (nice to have, but not required)

Have phlebotomy experience and are comfortable performing blood draws

Have strong medical knowledge and clinical understanding, including proficiency in medical terminology

Are passionate about contributing to clinical trials that impact global health

Why Centricity Research?

We connect people to scientific advancements through groundbreaking research within a deeply human experience.

Quality : Care : We show up for each other, our customers, and our mission - always going the extra mile.

One Team : We collaborate, support one another, and succeed together.

Grow for Valuable : We grow with purpose - to expand access to research and improve global health.

Comprehensive health, dental, and vision insurance

- Enhanced EAP – mental health support
- Flexible PTO + paid holidays
- 401(k) / RRSP with company match and immediate vesting

We’re an equal opportunity employer committed to building a diverse and inclusive workplace. Join the Centricity Research Team!

Centricity Research is one of the largest clinical research networks in North America. We are a 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.

📌 Clinical Research Coordinator - Full Time (Toronto)
🏢 Centricity Research
📍 Toronto