Registered Nurse (Casual-PRN)

Centricity Research • Toronto, ON

2d • Onsite

About The Position

We are looking for Registered Nurses (RNs) to support our Centricity Research team at our Etobicoke locations on a casual basis. In this role, you’ll provide clinical support for ongoing studies, with a strong focus on the safe preparation, handling, and administration of investigational products (IP). You’ll work closely with Investigators and the clinical research team to ensure study activities are conducted safely, accurately, and in compliance with protocol and regulatory requirements. This is a flexible, hands-on role ideal for nurses who enjoy working in a dynamic research environment and contributing to high-quality patient care.

Requirements

• Registered Nurse (RN) with an active, unencumbered license in Ontario.
• Proficient in medication preparation and intramuscular injections.
• Strong clinical skills, including phlebotomy and IV placement.
• Detail-oriented and committed to patient safety and protocol compliance.
• Comfortable working in a fast-paced, flexible, and team-oriented environment.
• Communicate clearly and professionally with patients and clinical teams.
• Adaptable and open to working on a casual, as-needed basis.

Nice To Haves

• Experience in acute care or clinical research (Phase I–IV experience is a plus).
• Active ACLS certification.

Responsibilities

• Ensure the safety, well-being, and positive experience of all study participants.
• Conduct study activities in accordance with protocols, GCP, SOPs, and local healthcare privacy regulations.
• Maintain a strong understanding of study protocols to ensure accurate execution of all study-related tasks.
• Perform nursing procedures including phlebotomy, IV placement, medication preparation, infusions, and injections.
• Prepare investigational product (IP) in accordance with protocol and Pharmacy Manual guidelines.
• Accurately dispense, track, and maintain inventory of investigational product and study supplies.
• Adhere to study blinding requirements and ensure proper handling of blinded materials.
• Support study visits by completing delegated clinical and administrative tasks under Investigator direction.
• Ensure timely and accurate documentation of source data, CRFs, queries, and CTMS updates.
• Maintain and update Investigator Site Files and other required study documentation.
• Communicate effectively with Investigators, research staff, and other stakeholders regarding study-related questions or updates.
• Build and maintain professional relationships with participants, physicians, sponsors, and vendors.
• Support additional research activities as needed.

Benefits

• 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.

What This Job Offers

• Career Level: Mid Level