What are the responsibilities and job description for the Clinical Research Coordinator I position at Centricity Research?
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 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
Our Mission
We connect people to scientific advancements through groundbreaking research within a deeply human experience.
Our Core Values
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.
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 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
- 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
- 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
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’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.