Clinical Research Coordinator I

Centricity Research•Toronto, ON

12d

About The Position

We are seeking a Clinical Research Coordinator I (CRC I) to join our research team. 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. This is an excellent opportunity to build your skills in clinical research and contribute to meaningful studies that impact patient care.

Requirements

Have a bachelor’s degree in a health, science, or research-related field (or equivalent combination of education and experience)
Understand basic medical terminology, or are eager to learn it quickly
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

Nice To Haves

2–4 years of experience in a healthcare setting and are comfortable with clinical tools like blood pressure monitors, ECG machines, and weight scales
Phlebotomy experience — or are open to learning it where permitted by law (we’ll provide the training).

Responsibilities

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
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)
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