Clinical Research Coordinator

Centricity Research•Toronto, ON

16d•CA$55,000 - CA$62,500•Onsite

About The Position

We are seeking an experienced, full-time, permanent Clinical Research Coordinator (CRC) to join our new Centricity Research Toronto LMC Multispecialty site team. 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 role is ideal for a proactive coordinator who can take ownership, adapt quickly, and contribute immediately in a growing team environment.

Requirements

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 hands-on phlebotomy experience and are currently qualified to perform phlebotomy in Canada.
Have strong knowledge of medical terminology, GCP, study protocols, SOPs, and clinical research documentation requirements.
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.
Communicate openly, collaborate effectively, and contribute positively to a new and growing site team.

Nice To Haves

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

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)
Support lab supply inventory, equipment maintenance, and administrative needs
Assist with community engagement and outreach events as needed