Clinical Research Coordinator I

Oshawa, ON
On-site
Posted Oct 17, 2026
1 position

$55,000–$62,500 / year

Opens an external site

Employment type: Full-time
Experience level: Mid-level · 2+ years
Minimum education: Bachelor’s degree
Posting language: English
Working hours: 40 hours per week

Job summary

Coordinate clinical study visits and participant activities while ensuring safety and compliance with protocols, Good Clinical Practice, standard operating procedures, and regulatory requirements. Maintain accurate study and regulatory records, support data quality checks and monitoring activities, and assist with site operations and start-up.

Job details

About the Role We are seeking an experienced full-time Clinical Research Coordinator I (CRC I) to join our research team, primarily based at our Oshawa site, with travel to and support for our TOLMC site as needed. In this role, you will provide additional CRC coverage and support continuity of clinical research operations while 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. Prior clinical research coordination experience and phlebotomy skills are required. What You’ll Do Study Coordination & Participant Safety 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 Recruitment, Screening & Enrollment 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 Study Execution & Data Integrity 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) Quality, Compliance & Site Support Prepare for monitoring visits, audits, and maintain regulatory files Perform regular quality control checks on source data and documents Support lab supply inventory, equipment maintenance, and administrative needs Assist with community engagement and outreach events as needed You 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 prior experience as a Clinical Research Coordinator and are comfortable with clinical tools like blood pressure monitors, ECG machines, and weight scales Have phlebotomy experience and are comfortable performing blood draws Understand basic medical terminology, or are eager to learn it quickly Are passionate about contributing to clinical trials that impact global health Are organized, detail-oriented, and skilled at multitasking in a fast-paced environment Are proactive, collaborative, and take ownership of your work Value open communication and thrive in a team-driven environment Are able to work primarily at our Oshawa site and travel to support our TOLMC site as needed Why 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 insurance Enhanced EAP – mental health support Flexible PTO + paid holidays Continuing education reimbursement 401(k) / RRSP with company match and immediate vesting Ready 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.

What you’ll do

Requirements

Requires prior clinical research coordination experience, phlebotomy skills, and comfort using clinical tools such as blood pressure monitors, ECG machines, and weight scales. A bachelor’s degree in a health, science, or research-related field, or an equivalent combination of education and experience, is sought, along with strong organization, attention to detail, and collaboration skills.