Clinical Research Coordinator 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 performing 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

• Conduct study visits in alignment with protocol, GCP, SOPs, and regulatory requirements
• Ensure participant safety and welfare, reporting and documenting adverse events per protocol and regulations
• Perform clinical tasks such as phlebotomy, ECGs, vitals, sample collection, processing, and investigational product handling

Recruitment, Screening & Enrollment

• 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 accurate documentation
• Schedule and coordinate study visits across the participant lifecycle

Study Execution & Data Integrity

• 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 by completing feasibility questionnaires (FQs) and actively participating in pre-study visits (PSVs) to ensure site preparedness and compliance

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:

Core Competencies

• Attention to Detail: Ensures accuracy and compliance in documentation and clinical tasks
• Organization & Time Management: Effectively balances multiple studies and deadlines
• Collaboration: Works well within a multidisciplinary team and communicates clearly with investigators, staff, and sponsors
• Participant-Centered Approach: Maintains participant safety and comfort as a top priority
• Adaptability: Adjusts quickly to changing study requirements and timelines

Skills & Experience

• 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)
• Phlebotomy experience is a plus (where permitted by law, we can provide training if you don’t already have it)
• Understand basic medical terminology, or are eager to learn it quickly