Clinical Research Coordinator I

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 play a dual role in supporting the success of our clinical studies. About half of your time will focus on patient recruitment - engaging with potential participants, guiding them through the screening process, and ensuring they have a positive experience from the very beginning. The other half will be spent on clinical responsibilities - performing study-related procedures, maintaining compliance with protocols, and working closely with Investigators to deliver high-quality research.

The CRC I is key to both sides of the research process: connecting people to studies and ensuring every step of the clinical journey is carried out smoothly, accurately, and on time.

This is a fully in-person, on-site role.

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)
• Enjoy building relationships and making participants feel comfortable and informed
• Are confident reaching out to potential participants, explaining studies clearly, and supporting enrollment goals
• Can balance people-facing recruitment activities with detailed, hands-on clinical responsibilities
• 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.