Coordonnateur(trice) de recherche clinique I / Clinical Research Coordinator I - RN (Bilingual)
Centricity Research Mirabel, Quebec, Canada

About this position
Rejoignez-nous chez Centricity Research !

Join Us at Centricity Research!

Centricity Research is one of the largest clinical research networks in North America. We area 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.

Clinical Research Coordinator I (RN Preferred) – ONSITE – Mirabel, Quebec

Location: Mirabel, Quebec, Canada

Work Arrangement: Full-time, 100% Onsite

Language Requirement: Fluent French required (spoken and written)

Please note: This is an onsite position based in Mirabel, Quebec. Remote or hybrid work is not available. Candidates must be legally eligible to work in Canada and able to commute to or relocate to the Mirabel area.

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, specimen 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 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

Required Qualifications

Active and unrestricted Registered Nurse (RN) or Licensed Practical Nurse (LPN) license in Quebec is mandatory

Minimum 1 year of nursing experience in a hospital, clinic, medical practice, research site, or healthcare setting

Proven experience performing phlebotomy (blood draws) independently is required

Must be comfortable performing clinical procedures including: blood draws / venipuncture, vital signs, ECGs, specimen collection, processing, and shipment, participant assessments and clinical documentation

Experience working directly with patients in a clinical environment is required

Strong knowledge of patient safety, confidentiality, and clinical documentation standards

Ability to work onsite five (5)



days per week at the Mirabel research site

Solid organizational skills with the ability to manage multiple priorities and meeting study timelines

Bilingualism (French and English) is strongly preferred

Preferred Qualifications

Previous clinical research experience as a Clinical Research Coordinator, Research Nurse, Clinical Trial Assistant, or similar role

Experience with informed consent, participant recruitment, study visits, and clinical trial documentation

Familiarity with ICH‑GCP guidelines and Health Canada regulations

Experience with electronic medical records (EMR), EDC systems, or clinical trial databases

Important Note

This position requires an active RN or LPN license and hands‑on phlebotomy experience. Candidates without nursing credentials or blood draw experience will not be considered.

Why Centricity Research?
Our Mission
We connect people to scientific advancements through groundbreaking research within an 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

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.

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📌 Coordonnateur(trice) de recherche clinique I / Clinical Research Coordinator I - RN (Bilingual)
🏢 Centricity Research
📍 Quebec City