Clinical Research Coordinator I - RN at Centricity Research

Mirabel, Quebec, Canada -

Full Time

Start Date

Immediate

Expiry Date

24 Aug, 26

Salary

0.0

Posted On

26 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Study Coordination, Participant Safety, Clinical Procedures, Phlebotomy, Patient Recruitment, Informed Consent, Data Integrity, Regulatory Compliance, GCP, SOPs, Quality Control, Medical Terminology, ECG Operation, Sample Processing, Site Start-up, Multitasking

Industry

Biotechnology Research

Description

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 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 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 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.

Responsibilities

The coordinator will manage clinical study visits, ensure participant safety, and handle recruitment and enrollment processes. They are also responsible for maintaining accurate study documentation and ensuring compliance with regulatory requirements and protocols.