Clinical Research Coordinator I

Centricity Research•Suffolk, VA

18d•Onsite

About The Position

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.

Requirements

Have a bachelor’s degree in a health, science, or research-related field (or equivalent combination of education and experience)
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

Nice To Haves

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

Responsibilities

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
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
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
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