Clinical Research Coordinator I - RN, Ahuntsic North
Clinical Research Coordinator I - RN, Ahuntsic North
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Ahuntsic North H2B, Canada
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Last edited: less than a week ago
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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:
Licensed Registered Nurse (RN) in good standing with a Canadian provincial regulatory body.
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.
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’rean 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
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:
Licensed Registered Nurse (RN) in good standing with a Canadian provincial regulatory body.
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.
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’rean 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
Highlights
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Company nameCentricity Research
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Job positionClinical Research Coordinator I - RN
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