Clinical Research Coordinator I

Centricity Research; Toronto; Sur place; CAD 55 000 - 63 000; Plein temps

Avantages offerts par ce poste

Comprehensive health, dental, and vis­

Enhanced EAP – mental health support

Flexible PTO + paid holidays

Continuing education reimbursement

401(k) / RRSP with company match andim

Résumé du poste

Centricity Research is seeking a full-time Clinical Research Coordinator I to join our team at the CPU Toronto location. You will support the successful execution of clinical studies by performing a mix of administrative and clinical responsibilities, collaborating with Investigators and the research team to ensure protocol compliance.

The ideal candidate has strong medical knowledge, phlebotomy experience, and 2–4 years in healthcare.

Qualifications

• Have a bachelor’s degree in a health, science, or research-related field (or equivalent combination of education and experience)
• Are an internationally 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
• Have phlebotomy experience and are comfortable performing blood draws
• Have strong medical knowledge and clinical understanding, including proficiency in medical terminology
• 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

Responsabilités

• 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
• 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
• 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)

Connaissances

Phlebotomy experience

Clinical knowledge

Multitasking in fast-paced environment

Organized and detail-oriented

Team collaboration

Formation

Bachelor’s degree in health/science or related field

Outils

ECG machines

Blood pressure monitors

Weight scales

Description du poste

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 strong 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)