Research Assistant

Centricity Research•Toronto, ON

16d•CA$45,000 - CA$50,000•Onsite

About The Position

We're looking for a full-time, permanent Research Assistant (RA) to join our Centricity Research Toronto LMC Multispecialty site and support the successful execution of clinical research studies from start to finish. In this hands-on role, you'll work closely with Investigators, Clinical Research Coordinators (CRCs), and the wider site team to recruit and support participants, conduct study visits, perform phlebotomy and other delegated clinical procedures, process samples, and maintain accurate study documentation. Your work will help ensure studies run safely, efficiently, and in compliance with protocols and regulatory requirements.

Requirements

At least 3 years of hands-on phlebotomy experience and are qualified to perform phlebotomy in Canada.
Previous clinical research experience, including exposure to study protocols, GCP, participant visits, and clinical research documentation.
A degree or diploma in biological sciences, medicine, healthcare, clinical research, or a related field, or an equivalent combination of relevant education and experience.
Comfortable using clinical equipment such as blood pressure monitors, ECG machines, and point-of-care testing devices.
Strong attention to detail and can maintain accurate, complete, and compliant documentation.
Communicate clearly and professionally with participants, colleagues, and external partners.
Self-motivated, adaptable, and able to work independently with minimal supervision while contributing to a collaborative team.
Bring a proactive, organized, and solutions-focused approach to changing priorities in a fast-paced environment.

Responsibilities

Conduct study activities in compliance with GCP, SOPs, and protocols; monitor participant safety; and perform scheduled visits and assessments (e.g., vitals, ECGs).
Support recruitment efforts, screen participants, obtain informed consent, and maintain accurate documentation.
Perform delegated clinical tasks such as phlebotomy, sample collection/shipping, point-of-care testing, and investigational product accountability.
Complete source documents and CRFs, maintain CTMS records, report adverse events promptly, and ensure investigational product inventory and storage compliance.
Prepare for monitoring visits and audits, maintain ISF, organize exam rooms and labs, assist with scheduling and participant check-in/out, and support outreach events.