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

The Clinical Research Coordinator I (CRC I) supports the successful execution of clinical studies by managing a mix of administrative and clinical tasks. This role works 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

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.

Education/Experience

Minimum:

  • CAN: College/University degree in a relevant field of science
  • US: HS/GED
  • CAN/US: Depending on role requirements, specific degree and licensure from designated provincial/state body the location of the clinical site (ex. RN, MLT, etc.)
  • Active BLS certification (for CPU setting)
  • Proficient IV and phlebotomy skills (as applicable to the site requirements)

Preferred

  • Experience working in a healthcare environment e.g. blood pressure sphygmometers, automated blood pressure machines, weight scales, and ECG machines
  • Knowledge of medical terminology
  • Phlebotomy experience an asset
  • Active ACLS certification (for CPU setting)

Core Competencies/Skills

Prerequisite (Essential):

  • Excellent communication skills (verbal and written)
  • Excellent computer skills (MS Word, Excel and Outlook)
  • Attention to detail
  • Ability to manage time efficiently
  • Self-directed
  • Teamwork & Collaboration
  • Proficient level of clinical, interpretive, and analytical skills with organizational skills for project planning
  • Flexible & Adaptable
  • Strong knowledge of ICH GCP, FDA & HC Division 5 guidelines

Foundation

  • Conflict resolution
  • Receptive to feedback
  • Empowering & Developing others
  • Empathy Skills
  • Planning and organizing skills
  • Excellent problem-solving skills
  • Achievement oriented
  • Analytical ability
  • Initiative
  • Decision making

Leadership

  • Forward thinking
  • Innovative
  • Creative
  • Strategic thinking
  • Self confidence
  • Strong interpersonal skills

PHYSICAL DEMANDS

  • Physical demands include but not limited to prolonged sitting, light lifting, standing, reaching, walking, and bending.
  • Frequently required to complete work on the computer in a seated position
  • May be required to lift light boxes (10 - 20lbs)

WORKING CONDITIONS

  • Modern medical office environment or home office environment
  • Required to follow OSHA and CCOHS guidelines, in addition to other local healthcare regulations
  • Required to perform duties in relation to HIPAA, PIDEDA, and other local privacy regulations
  • Some positions and locations may require work to be done outside of regular business hours (which may include overnights, weekends, & holidays) [CLBHC1]

Benefits

  • Opportunities to work with internationally renowned physicians
  • Comprehensive health benefits, competitive salary
  • RRSP or 401(k) contribution matching
  • Continued opportunities for growth & development; yearly education allowance
  • Paid holiday closures and employee appreciation days off

[CLBHC1]Apply to JD template for all roles - thinking lab, study admin, RA, SI, etc. Many roles that could be asked to support. [CLBHC1]
Posted 2025-08-22

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