Clinical Research Coordinator I

1 week ago

PointeClaire, Canada Centricity Research Full time

Clinical Research Coordinator I Join to apply for the Clinical Research Coordinator I role at Centricity Research. Montreal, Quebec, Canada CA$20.77-CA$31.59 1 day ago About the Role We’re looking for a Clinical Research Coordinator I to support the successful execution of clinical studies by managing a mix of administrative and clinical tasks. In this role, you will work closely with investigators to ensure study activities are organized, compliant, and aligned with protocol requirements. What You’ll Do Study Coordination & Participant Safety Ensure the safety and well‑being of all study participants Conduct study visits in line with protocol, GCP, and internal SOPs Collect study‑specific assessments (e.g., vitals, ECGs) and maintain documentation accuracy Obtain and maintain proper informed consent Recruitment, Screening & Enrollment Promote and support recruitment initiatives to identify eligible study participants Screen participants according to protocol inclusion/exclusion criteria Guide participants through the consent process and ensure proper documentation Schedule and coordinate study visits across the full lifecycle of participation Study Execution & Data Collection Perform clinical tasks such as phlebotomy, sample processing/shipping, point‑of‑care testing, and participant monitoring Accurately complete source documentation, CRFs, queries, and maintain CTMS records Dispense and track investigational products according to protocol Collect and report adverse events, including timely SAE reporting Participate in site feasibility questionnaires (FQs) and pre‑study visits (PSVs) to support site readiness and study start‑up activities 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 Qualifications 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 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 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 Seniority level Entry level Employment type Other Job function Research, Analyst, and Information Technology 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. #J-18808-Ljbffr

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