Impress employers and recruiters.
Choose from hundreds of resume examples.
Impress employers and recruiters.
Choose from hundreds of resume examples.
Tailor your resume to this Clinical Research Coordinator I role.
Rezi rewrites your resume against Centricity Research's job description. Free.
Tailor your resume to this Clinical Research Coordinator I role.
Rezi rewrites your resume against Centricity Research's job description. Free.
Don't guess if your resume is good enough.
See how it scores against the Clinical Research Coordinator I posting at Centricity Research — free, in seconds.
Don't guess if your resume is good enough.
See how it scores against the Clinical Research Coordinator I posting at Centricity Research — free, in seconds.
About the Role
We are seeking a full-time Clinical Research Coordinator I (CRC I) to support the successful execution of clinical studies by performing 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. Strong medical knowledge, clinical understanding, and phlebotomy experience are required. An international medical graduate (IMG) or internationally trained physician is preferred.
Responsibilities
- 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, phlebotomy, sample collection/processing, and investigational product handling
- 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
- 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)
- 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
Requirements
- Have a bachelor’s degree in a health, science, or research-related field (or equivalent combination of education and experience)
- Are an international medical graduate (IMG) or internationally trained physician (preferred)
- 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 and are comfortable performing blood draws
- Have strong medical knowledge and clinical understanding, including proficiency in medical terminology
- 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
Skills
- Phlebotomy
- Medical knowledge
- Clinical understanding
- Medical terminology
- GCP
- SOPs
- Blood pressure monitors
- ECG machines
- Weight scales
Location
- Toronto
Work Type
- Full-time
Experience Level
- 2-4 years
Education Level
- Bachelor's degree in a health, science, or research-related field
- International medical graduate (IMG) or internationally trained physician
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
About the Company
- 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.
Equal Opportunity
- 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.