Clinical Research Coordinator I

Centricity Research
Suffolk, VA
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) for our Suffolk, VA site 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.

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.
Posted 2025-11-12

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