Clinical Research Coordinator I

Clinical Research Coordinator I (CRC I) - Part-Time

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 part-time 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
• Participate in site feasibility questionnaires (FQs) and pre-study visits (PSVs) to support site readiness and study start-up activities

 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.

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.