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.

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.

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, phlebotomy, 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

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

You Might Be a Great Fit If You:

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 robust medical knowledge and clinical understanding,



including proficiency in medical terminology

Are passionate about contributing to clinical trials that impact global health

Are organized, detail-oriented, and skilled at multitasking in a fast-paced environment

Are proactive, collaborative, and take ownership of your work

Value open communication and thrive in a team-driven environment

Why Centricity Research?
Our Mission
We connect people to scientific advancements through groundbreaking research within a deeply human experience.

Our Core Values

Quality : We aim for excellence and integrity in everything we do - because lives depend on it.

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

Be the Change You Seek : We're adaptable, forward-thinking, and constantly improving - for the betterment of all.

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

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

Own It : We take initiative, deliver results, and follow through - with passion and accountability.

Comprehensive health, dental, and vision insurance

Enhanced EAP – mental health support

Flexible PTO + paid holidays

Continuing education reimbursement

401(k) / RRSP with company match and immediate vesting

We’re an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and will provide accommodations during the hiring process upon request.

The pay range for this role is:

55,000 - 62,500 CAD per year (Centricity Research CPU Toronto)

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📌 Clinical Research Coordinator I (Ontario)
🏢 Centricity Research
📍 Ontario