Job Description
Clinical Research Coordinator I (CRC I) Join Us at Centricity Research! Centricity Research is one of the largest clinical research networks in North America. We are a 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.
About The Role We’re looking for a Clinical Research Coordinator I (CRC I) to support the successful execution of clinical studies by managing a mix of administrative and clinical tasks. In this role, you’ll work closely with Investigators to ensure study activities are organized, compliant, and aligned with protocol requirements. The CRC I brings strong attention to detail and a solid grasp of study protocols, helping keep research operations running smoothly, accurately, and on time.
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
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.
Job Tags
Immediate start, Flexible hours,