Research Assistant

Centricity Research; Toronto; On-site; CAD 45,000 - 50,000; Full time

Job summary

Centricity Research Toronto LMC Multispecialty is seeking a full-time Research Assistant to support clinical trials from start to finish. You will recruit participants, conduct visits, perform phlebotomy, process samples, and maintain study documentation in a fast-paced team environment.

The role requires hands-on phlebotomy experience in Canada, plus familiarity with GCP and protocol adherence. A biology/healthcare degree or equivalent is expected, and a collaborative, detail-oriented approach

Qualifications

• Must have at least 3 years of hands-on phlebotomy experience and be qualified to perform phlebotomy in Canada.
• Experience in clinical research, including study protocols, GCP, participant visits, and documentation.
• Degree or diploma in biological sciences, medicine, healthcare, or related field, or equivalent experience.

Responsibilities

• Conduct study visits and phlebotomy; collect samples and document procedures according to protocol.
• Recruit and support participants, obtain informed consent, and ensure accurate study documentation.
• Maintain CTMS records, assist with monitoring visits and audits, and ensure regulatory compliance.

Skills

Phlebotomy

Clinical research experience

Attention to detail

Communication

Independent work

Education

Biological sciences/medicine/healthcare degree or diploma

Tools

ECG & BP devices

Job description

Centricity Research is one of the largest clinical research networks in North America. We area 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'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.

Compensation

Base salary range: $45,000-$50,000. This role is eligible for incentive compensation.

What you'll do

• Study Protocol & Safety: Conduct study activities in compliance with GCP, SOPs, and protocols; monitor participant safety; and perform scheduled visits and assessments (e.g., vitals, ECGs).
• Recruitment & Enrollment: Support recruitment efforts, screen participants, obtain informed consent, and maintain accurate documentation.
• Study Visit Execution: Perform delegated clinical tasks such as phlebotomy, sample collection/shipping, point‑of‑care testing, and investigational product accountability.
• Data Integrity & Compliance: Complete source documents and CRFs, maintain CTMS records, report adverse events promptly, and ensure investigational product inventory and storage compliance.
• Site & Administrative Support: 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.

You Might Be a Great Fit If You:

• Have at least 3 years of hands‑on phlebotomy experience and are qualified to perform phlebotomy in Canada.
• Have previous clinical research experience, including exposure to study protocols, GCP, participant visits, and clinical research documentation.
• Have a degree or diploma in biological sciences, medicine, healthcare, clinical research, or a related field, or an equivalent combination of relevant education and experience.
• Are comfortable using clinical equipment such as blood pressure monitors, ECG machines, and point‑of‑care testing devices.
• Have strong attention to detail and can maintain accurate, complete, and compliant documentation.
• Communicate clearly and professionally with participants, colleagues, and external partners.
• Are 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.

The pay range for this role is:

45,000 - 50,000 CAD per year (Centricity Research Toronto LMC Multispecialty)