Join Us at Centricity Research!
Centricity Research is one of the largest clinical research networks in North America. We area 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 ClinicalResearch CoordinatorI(CRCI) supports the successful execution of clinical studies byperforminga mix of administrative and clinical tasks. This role works closely with Investigators to ensure study activities are organized, compliant, and aligned with protocol requirements. TheCRCIbrings 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
- Ensureparticipantsafety and welfare, reporting and documenting adverse eventsperprotocol and regulations
- Perform clinical tasks such as phlebotomy, ECGs, vitals, sample collection, processing, and investigational product handling
Recruitment, Screening & Enrollment
- Support recruitment strategies toidentifyand enroll eligible participants
- Conduct participant screening according to protocol inclusion/exclusion criteria
- Guide participants through the informed consent process and ensureaccuratedocumentation
- Schedule and coordinate study visits across the participant lifecycle
Study Execution & DataIntegrity
- 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 activelyparticipatingin pre-study visits (PSVs) to ensure site preparedness and compliance
Quality, Compliance & Site Support
- Prepare for monitoring visits, audits, andmaintainregulatory files
- Perform regular quality control checks on source data and documents
- Support lab supply inventory, equipment maintenance, and administrative needs
- Assistwith 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:Maintainsparticipant 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 notrequired)
- Phlebotomy experience is a plus(wherepermittedby law, we can provide training if youdon’talready have it)
- Understand basic medical terminology, or are eager to learn it quickly
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