Join Us at Centricity Research!
Centricity Research is one of the largest clinical research networks in North America. We are a 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 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.
What you'll do
Study Coordination & Participant Safety
Conduct study visits in accordance with protocol, GCP, SOPs, and regulatory requirementsEnsure participant safety and well-being, reporting and documenting adverse events per protocol and regulationsPerform clinical procedures such as vitals, ECGs, sample collection/processing, and investigational product handlingRecruitment, Screening & Enrollment
Support recruitment strategies to identify and enroll eligible participantsConduct participant screening according to protocol inclusion/exclusion criteriaGuide participants through the informed consent process and ensure proper documentationSchedule and coordinate study visits throughout the participant lifecycleStudy Execution & Data Integrity
Accurately complete study documentation, regulatory records, and periodic reportsPrepare for and support monitoring visits, audits, and inspectionsPerform regular quality control (QC) checks on study data and source documentsCollaborate with investigators, management, and sponsors to ensure study compliance and accuracyContribute to site start-up activities, including feasibility questionnaires (FQs) and pre-study visits (PSVs)Quality, Compliance & Site Support
Prepare for monitoring visits, audits, and maintain regulatory filesPerform regular quality control checks on source data and documentsSupport lab supply inventory, equipment maintenance, and administrative needsAssist with community engagement and outreach events as neededYou Might Be a Great Fit If You:
Have a bachelor’s degree in a health, science, or research-related field (or equivalent combination of education and experience)Have 2–4 years of experience in a healthcare setting and are comfortable with clinical tools like blood pressure monitors, ECG machines, and weight scales (nice to have, but not required)Have phlebotomy experience — or are open to learning it where permitted by law (we’ll provide the training). Understand basic medical terminology, or are eager to learn it quicklyAre passionate about contributing to clinical trials that impact global healthAre organized, detail-oriented, and skilled at multitasking in a fast-paced environmentAre proactive, collaborative, and take ownership of your workValue open communication and thrive in a team-driven environmentWhy Centricity Research?
Our Mission
We connect people to scientific advancements through groundbreaking research within a deeply human experience.
Our Core Values
Quality: We aim for excellence and integrity in everything we do - because lives depend on it.Care: We show up for each other, our customers, and our mission - always going the extra mile.Be the Change You Seek: We're adaptable, forward-thinking, and constantly improving - for the betterment of all.One Team: We collaborate, support one another, and succeed together.Grow for Good: We grow with purpose - to expand access to research and improve global health.Own It: We take initiative, deliver results, and follow through - with passion and accountability.Benefits
Comprehensive health, dental, and vision insuranceEnhanced EAP – mental health supportFlexible PTO + paid holidaysContinuing education reimbursement401(k) / RRSP with company match and immediate vestingReady to Apply?
We’d love to hear from you – apply now!
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.
PIda3df4655c0c-30511-40363123
Clinical Research Coordinator I • Toronto, Ontario, Canada, M4G 3E8
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